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.

Common aneuploidy testing NIPT

Clinical Indication ID & Name

R445

Common aneuploidy testing NIPT

Test Group

Prenatal

Test code

R445.1

Test name

N/A

Target genes

Chromosomes 13, 18 and 21

Test scope

n/a

Test method/ technology

NIPT

Optimal Family Structure

n/a

Eligibility Criteria

Any previous pregnancy with reported full trisomy of chromosomes 13, 18 or 21, meeting the following criteria:
Inclusion:
•From 10 weeks (gestational age confirmed by dating scan) and up to 21 weeks and 6 days (21+6) of pregnancy.
•Two attempts at NIPT per pregnancy can be offered.
Exclusion:
• Maternal cancer (unless in remission)
• Blood transfusion in the last 4 months (whole blood or plasma)
•Bone marrow or organ transplant recipient
•Vanished twin pregnancy (an empty second pregnancy sac or a second pregnancy sac containing non-viable fetus)
•Maternal T21
•Maternal balanced translocation or mosaicism of T21, T18 or T13
•Immunotherapy in the current pregnancy, excluding IVIg treatment
•Stem cell therapy
•Previous pregnancy was not a full trisomy (reciprocal translocation or partial trisomy)
•The current pregnancy was conceived using a donor egg (unless the egg for this pregnancy is from the same egg donor used in a previous pregnancy diagnosed with Down’s, Edward’s or Patau’s syndrome)

For any enqueries relating to referring samples contact: thesafetest@stgeorges.nhs.uk

Commissioning group

Core

Overlapping idications

R401 Common aneuploidy testing – prenatal should be used where amniocentesis or Chorionic villus sampling (CVS) taken.

Address for samples/request forms

Please refer to the test request form.

Contact with queries

gos-tr.norththamesgenomics@nhs.net

Supporting documents

n/a

Education resources

n/a

Service updates

n/a

Request form download

Form not available, please contact us to enquire.

Consent record

See consent guidance in test request form

Sample requirements

n/a