Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Carrier Screening - Comprehensive Panel (145 Genes) Genesys Diagnostics Genesys Diagnostics, Inc. United States | 185 | 145 |
|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
GJB2 - NGS including CNV analysis Centogene US, LLC - The Rare Disease Company United States | 7 | 1 |
|
GJB2 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 7 | 1 |
|
Invitae Congenital Ichthyosis Panel Invitae United States | 77 | 45 |
|
Invitae Comprehensive Deafness Panel Invitae United States | 405 | 219 |
|
Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics United States | 288 | 218 |
|
GJB2 Regulatory Element Deletion Testing (GJB6-D13S1830 and GJB6-D13S1854) PreventionGenetics United States | 7 | 1 |
|
Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
|
Hereditary Hearing Loss and Deafness Panel PreventionGenetics United States | 356 | 211 |
|
Molecular Vision Laboratory United States | 342 | 268 |
|
Molecular Diagnostics Children's Hospital of Wisconsin United States | 9 | 5 |
|
Invitae Ectodermal Dysplasia and Related Disorders Panel Invitae United States | 148 | 73 |
|
GJB2 Sequence Analysis (Prenatal Diagnosis) Baylor Genetics United States | 7 | 1 |
|
GJB2 Sequence Analysis (Familial Mutation/Variant Analysis) Baylor Genetics United States | 7 | 1 |
|
Baylor Genetics United States | 7 | 1 |
|
GJB2 Deletion/Duplication Analysis (Prenatal Diagnosis) Baylor Genetics United States | 7 | 1 |
|
GJB2 Deletion/Duplication Analysis Baylor Genetics United States | 7 | 1 |
|
Connexin Test (GJB2 Sequencing and DFNB1 (GJB6) Deletions) Laboratory for Molecular Medicine Mass General Brigham Personalized Medicine United States | 6 | 2 |
|
PreventionGenetics United States | 6 | 1 |
|
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.