Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics United States | 288 | 218 |
|
Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel Otogenetics United States | 123 | 129 |
|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
POU3F4 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 203 | 194 |
|
Invitae Congenital Ichthyosis Panel Invitae United States | 77 | 45 |
|
Invitae Epidermolysis Bullosa and Palmoplantar Keratoderma Panel Invitae United States | 95 | 45 |
|
Invitae Comprehensive Deafness Panel Invitae United States | 405 | 219 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Invitae Broad Carrier Screen without X-linked Disorders Invitae United States | 195 | 98 |
|
Invitae United States | 224 | 112 |
|
Invitae Comprehensive Carrier Screen Invitae United States | 886 | 547 |
|
Hereditary Hearing Loss and Deafness Panel PreventionGenetics, part of Exact Sciences United States | 360 | 222 |
|
Molecular Vision Laboratory United States | 342 | 268 |
|
Invitae Ectodermal Dysplasia and Related Disorders Panel Invitae United States | 148 | 73 |
|
Deafness, X-Linked 2 (DFNX2) via the POU3F4 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
POU3F4 Sequence Analysis (Prenatal Diagnosis) Baylor Genetics United States | 1 | 1 |
|
POU3F4 Sequence Analysis (Familial Mutation/Variant Analysis) Baylor Genetics United States | 1 | 1 |
|
Baylor Genetics United States | 1 | 1 |
|
Laboratory for Molecular Medicine Mass General Brigham Personalized Medicine United States | 1 | 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.