Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
ZDHHC9 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Ophthalmology Eyes Vision Panel NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
CNGA3 Gene Achromatopsia type 2 NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
Laboratory of Human Genetics GENOMED Health Care Center Poland | 1 | 13 |
|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
CNGA3 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 417 | 413 |
|
PreventionGenetics, part of Exact Sciences United States | 285 | 137 |
|
Labcorp Genetics (formerly Invitae) LabCorp United States | 7 | 8 |
|
Leber congenital amaurosis and related disorders Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 20 | 32 |
|
Leber congenital amaurosis and related disorders NGS panel HNL Genomics Connective Tissue Gene Tests United States | 20 | 32 |
|
Leber congenital amaurosis and related disorders Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 20 | 32 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Invitae Inherited Retinal Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 486 | 293 |
|
Amplexa Genetics Amplexa Genetics A/S Denmark | 1 | 40 |
|
Amplexa Genetics Amplexa Genetics A/S Denmark | 1 | 10 |
|
Molecular Vision Laboratory United States | 342 | 268 |
|
Leber congenital amaurosis and related disorders NGS panel HNL Genomics Connective Tissue Gene Tests United States | 20 | 32 |
|
Leber congenital amaurosis and related disorders Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 20 | 32 |
|
Leber congenital amaurosis and related disorders Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 20 | 32 |
|
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.