Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Invitae United States | 160 | 62 |
|
Variant Resolution Test for CustomNext-Cancer® (+RNAinsight®) Ambry Genetics United States | 147 | 18 |
|
Variant Resolution Test for MelanomaNext® (+RNAinsight®) Ambry Genetics United States | 40 | 3 |
|
Hereditary Hearing Loss and Deafness Panel PreventionGenetics, part of Exact Sciences United States | 360 | 222 |
|
Anterior Segment Dysgenesis Disorders Panel PreventionGenetics, part of Exact Sciences United States | 272 | 278 |
|
Ambry Genetics United States | 40 | 9 |
|
Ambry Genetics United States | 147 | 91 |
|
Ambry Genetics United States | 122 | 71 |
|
Waardenburg syndrome Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 8 | 7 |
|
Waardenburg syndrome Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 8 | 7 |
|
Waardenburg syndrome NGS panel HNL Genomics Connective Tissue Gene Tests United States | 8 | 7 |
|
Invitae Microphthalmia, Anophthalmia, Coloboma (MAC) and Anterior Segment Dysgenesis Panel Invitae United States | 130 | 81 |
|
Genetic Services Laboratory University of Chicago United States | 26 | 68 |
|
PreventionGenetics, part of Exact Sciences United States | 12 | 6 |
|
Waardenburg Syndrome Type IIA via the MITF Gene PreventionGenetics, part of Exact Sciences United States | 4 | 1 |
|
Dhiti Omics Technologies Private Ltd India | 136 | 84 |
|
Waardenburg Syndrome (NGS Panel and Copy Number Analysis) MNG Laboratories (Medical Neurogenetics, LLC.) United States | 10 | 7 |
|
Waardenburg syndrome: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 10 | 7 |
|
Syndromic Hearing Loss NGS Panel Fulgent Genetics United States | 223 | 83 |
|
Comprehensive Hearing Loss NGS Panel Fulgent Genetics United States | 332 | 167 |
|
IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.