Request / Find a Test Tool

The National Genomic Test Directories specify which genomic tests are commissioned by the NHS in England, to be delivered by Genomic Laboratory Hubs.

This tool allows clinical teams to search all of the genomic tests available to patients through the National Testing Directory. From here you can find out more details about each test and information about how to order them. These tests can only be ordered by clinical teams, if you are a patient looking to request a test please speak to your clinical team directly.

Myeloproliferative Neoplasm

Clinical Indication ID & Name

M85

Myeloproliferative Neoplasm

Test Group

Haematology

Specialties

Test code

M85.1

Test name

Multi-target NGS limited panel - small variant (JAK2, CALR, MPL)

Target genes

JAK2, CALR, MPL

Test scope

Small variant detection

Test method/ technology

Panel

Optimal Family Structure

n/a

Eligibility Criteria

MPN diagnostic panel Myeloproliferative neoplasm Myeloproliferative neoplasm or suspected Myeloproliferative Neoplasm (diagnostic setting only) Small variant detection JAK2, CALR, MPL Panel Core Core

Test code

M85.2

Test name

Multi-target NGS panel - small variant (KRAS, NRAS, TP53, JAK2, CALR, MPL, ASXL1, CBL, CSF3R, CUX1, DNMT3A, EZH2, IDH1, IDH2, IKZF1, KIT, NFE2, SF3B1, SH2B3, SRSF2, TET2, U2AF1, HRAS, RUNX1, SETBP1, ZRSR2)

Target genes

KRAS, NRAS, TP53, JAK2, CALR, MPL, ASXL1, CBL, CSF3R, CUX1, DNMT3A, EZH2, IDH1, IDH2, IKZF1, KIT, NFE2, SF3B1, SH2B3, SRSF2, TET2, U2AF1, HRAS, RUNX1, SETBP1, ZRSR2

Test scope

Small variant detection

Test method/ technology

Panel

Optimal Family Structure

n/a

Eligibility Criteria

Myeloproliferative neoplasm or suspected Myeloproliferative Neoplasms (selected cases)

Test code

M85.3

Test name

Karyotype (To include detection of complex karyotype, cryptic deletion of 4q12, trisomy 8, -7/7q, -5/5q, i(17q), 12p- & t(9;22)(q34;q11) BCR-ABL1, del(4)(q12q12) FIP1L1-PDGFRA, other PDGFRA rearrangements, t(5;12)(q33;p13) ETV6-PDGFRB, other PDGFRB rearrangements, FGFR1 rearrangements, t(8;9)(p22;p24) PCM1-JAK2, inv(3)MECOM, 11q23, rearrangements of ABL1, JAK2, FLT3, RET, NTRK3)

Target genes

To include detection of complex karyotype, cryptic deletion of 4q12, trisomy 8, -7/7q, -5/5q, i(17q), 12p- & t(9;22)(q34;q11) BCR-ABL1, del(4)(q12q12) FIP1L1-PDGFRA, other PDGFRA rearrangements, t(5;12)(q33;p13) ETV6-PDGFRB, other PDGFRB rearrangements, FGFR1 rearrangements, t(8;9)(p22;p24) PCM1-JAK2, inv(3), 11q23, rearrangements of ABL1, JAK2, FLT3, RET, NTRK3

Test scope

Copy number variant detection to genomewide resolution; Structural variant detection

Test method/ technology

Karyotype or equivalent

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Test code

M85.5

Test name

FISH copy number and rearrangement Other: See tests M85.18 -M85.34 for individual specified FISH targets.

Target genes

Other: See tests M85.18 -M85.34 for individual specified FISH targets.

Test scope

Copy number variant detection to genomewide resolution; Structural variant detection

Test method/ technology

FISH

Optimal Family Structure

n/a

Eligibility Criteria

Myeloproliferative neoplasm (eosinophilia) or suspected Myeloproliferative Neoplasm (eosinophilia)

Test code

M85.7

Test name

FIP1L1-PDGFRA (4q12) FISH/RT-PCR

Target genes

FIP1L1-PDGFRA (4q12)

Test scope

Structural variant detection

Test method/ technology

FISH/Simple targeted mutation testing

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Test code

M85.8

Test name

FIP1L1-PDGFRA RT-qPCR

Target genes

FIP1L1-PDGFRA

Test scope

Structural variant detection

Test method/ technology

QF-PCR or equivalent

Optimal Family Structure

n/a

Eligibility Criteria

Myeloproliferative neoplasm (eosinophilia) or suspected Myeloproliferative Neoplasm (eosinophilia)

Test code

M85.9

Test name

ETV6-PDGFRB FISH/RT-PCR

Target genes

ETV6-PDGFRB

Test scope

Structural variant detection

Test method/ technology

FISH/Simple targeted mutation testing

Optimal Family Structure

n/a

Eligibility Criteria

Myeloproliferative neoplasm (eosinophilia) or suspected Myeloproliferative Neoplasm (eosinophilia)

Test code

M85.10

Test name

PCM1-JAK2 FISH/RT-PCR

Target genes

PCM1-JAK2

Test scope

Structural variant detection

Test method/ technology

FISH/Simple targeted mutation testing

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Test code

M85.11

Test name

BCR-ABL1 multiplex

Target genes

BCR-ABL1

Test scope

Structural variant detection

Test method/ technology

Simple targeted mutation testing

Optimal Family Structure

n/a

Eligibility Criteria

Suspected myeloproliferative neoplasm other than CML

Test code

M85.12

Test name

Other RT-PCR

Target genes

Dependent on clinical indication or specified request

Test scope

Structural variant detection

Test method/ technology

RT-PCR

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Test code

M85.13

Test name

WGS Germline and Tumour

Target genes

All including burden / signature

Test scope

All variant types

Test method/ technology

WGS

Optimal Family Structure

n/a

Eligibility Criteria

For paediatric patients only

Test code

M85.14

Test name

JAK2 V617F hotspot

Target genes

JAK2

Test scope

Small variant detection

Test method/ technology

Simple targeted mutation testing

Optimal Family Structure

n/a

Eligibility Criteria

Suspected myeloproliferative neoplasm other than CML

Test code

M85.15

Test name

JAK2 exon 12 hotspot

Target genes

JAK2

Test scope

Small variant detection

Test method/ technology

Simple targeted mutation testing

Optimal Family Structure

n/a

Eligibility Criteria

Suspected myeloproliferative neoplasm other than CML

Test code

M85.16

Test name

CALR exon 9 hotspot

Target genes

CALR exon 9 hotspot

Test scope

Small variant detection

Test method/ technology

Single gene sequencing

Optimal Family Structure

n/a

Eligibility Criteria

Suspected myeloproliferative neoplasm other than CML

Test code

M85.17

Test name

MPL exon 10 hotspot

Target genes

MPL

Test scope

Small variant detection

Test method/ technology

Simple targeted mutation testing

Optimal Family Structure

n/a

Eligibility Criteria

Suspected myeloproliferative neoplasm other than CML

Test code

M85.19

Test name

Chr8 copy number FISH

Target genes

Chr8

Test scope

Copy number variant detection to genomewide resolution

Test method/ technology

FISH

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Test code

M85.20

Test name

Chr7/Chr7q copy number FISH

Target genes

Chr7/chr7q

Test scope

Copy number variant detection to genomewide resolution

Test method/ technology

FISH

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Test code

M85.21

Test name

Chr5/Chr5q copy number FISH

Target genes

Chr5/chr5q

Test scope

Copy number variant detection to genomewide resolution

Test method/ technology

FISH

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Test code

M85.22

Test name

i(17q) FISH

Target genes

Chr17q

Test scope

Copy number variant detection to genomewide resolution; Structural variant detection

Test method/ technology

FISH

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Test code

M85.23

Test name

Chr12p copy number FISH

Target genes

Chr12p

Test scope

Copy number variant detection to genomewide resolution

Test method/ technology

FISH

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Test code

M85.24

Test name

t(9;22)(q34;q11) BCR-ABL1 FISH

Target genes

BCR-ABL1

Test scope

Structural variant detection

Test method/ technology

FISH

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Test code

M85.25

Test name

PDGFRA rearrangement FISH (other than FIP1L1-PDGFRA see M85.7)

Target genes

PDGFRA

Test scope

Structural variant detection

Test method/ technology

FISH

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Test code

M85.26

Test name

PDGFRB rearrangement FISH (other than ETV6-PDGFRB see M85.9)

Target genes

PDGFRB

Test scope

Structural variant detection

Test method/ technology

FISH

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Test code

M85.27

Test name

FGFR1 rearrangement FISH

Target genes

FGFR1

Test scope

Structural variant detection

Test method/ technology

FISH

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Test code

M85.28

Test name

JAK2 rearrangement FISH (other than PCM1-JAK2 see M85.10)

Target genes

JAK2

Test scope

Structural variant detection

Test method/ technology

FISH

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Test code

M85.29

Test name

inv(3)/t(3;3) FISH

Target genes

MECOM

Test scope

Structural variant detection

Test method/ technology

FISH

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Test code

M85.30

Test name

11q23 rearrangement FISH

Target genes

KMT2A

Test scope

Structural variant detection

Test method/ technology

FISH

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Test code

M85.31

Test name

ABL1 rearrangement FISH (other than BCR-ABL1 see M85.24)

Target genes

ABL1

Test scope

Structural variant detection

Test method/ technology

FISH

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Test code

M85.32

Test name

FLT3 rearragement FISH

Target genes

FLT3

Test scope

Structural variant detection

Test method/ technology

FISH

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Test code

M85.33

Test name

RET rearrangement FISH

Target genes

RET

Test scope

Structural variant detection

Test method/ technology

FISH

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Test code

M85.34

Test name

NTRK3 rearrangement FISH

Target genes

NTRK3

Test scope

Structural variant detection

Test method/ technology

FISH

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Test code

M85.35

Test name

Multi-target NGS panel - structural variant (to include t(9;22)(q34;q11) BCR-ABL1, del(4)(q12q12) FIP1L1-PDGFRA, other PDGFRA rearrangements, t(5;12)(q33;p13) ETV6-PDGFRB, other PDGFRB rearrangements, FGFR1 rearrangements, t(8;9)(p22;p24) PCM1-JAK2, inv(3), 11q23, rearrangements of ABL1, JAK2, FLT3, RET, NTRK3)

Target genes

t(9;22)(q34;q11) BCR-ABL1, del(4)(q12q12) FIP1L1-PDGFRA, other PDGFRA rearrangements, t(5;12)(q33;p13) ETV6-PDGFRB, other PDGFRB rearrangements, FGFR1 rearrangements, t(8;9)(p22;p24) PCM1-JAK2, inv(3), 11q23, rearrangements of ABL1, JAK2, FLT3, RET, NTRK3

Test scope

Structural variant detection

Test method/ technology

Panel

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Test code

M85.36

Test name

Multi-target NGS panel - copy number variant (cryptic deletion of 4q12, trisomy 8, -7/7q, -5/5q, i(17q), 12p-)

Target genes

Chr4q12, Chr8, Chr7/Chr7q, Chr5/Chr5q, Chr17q, Chr12p

Test scope

Copy number variant detection to genomewide resolution

Test method/ technology

Panel

Optimal Family Structure

n/a

Eligibility Criteria

Molecular assessment will aid diagnosis or management

Commissioning group

n/a

Overlapping idications

n/a

Address for samples/request forms

North Thames GLH, Rare & Inherited Disease Genomic Laboratory
Specimen Reception, Level 5 Barclay House, 37 Queen Square,
London WC1N 3BH

Contact with queries

rmh-tr.moleculardiagnostics@nhs.net

Supporting documents

Cancer WGS Clinician pack

Education resources

n/a

Service updates

n/a

Request form download

n/a

Consent record

See consent guidance in test request form

Sample requirements

See sample guidance in test request form