Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Genomic Unity® Hearing Loss Disorders Analysis Variantyx, Inc. United States | 1 | 318 |
|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
VCAN - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 417 | 413 |
|
Connective Tissue and Related Disorder Panel Centogene AG - the Rare Disease Company Germany | 75 | 76 |
|
Centogene AG - the Rare Disease Company Germany | 740 | 728 |
|
Centogene AG - the Rare Disease Company Germany | 203 | 194 |
|
PreventionGenetics, part of Exact Sciences United States | 285 | 137 |
|
Invitae Comprehensive Deafness Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 405 | 219 |
|
Invitae Stickler Syndrome Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 32 | 9 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins University, School of Medicine United States | 33 | 10 |
|
Invitae Inherited Retinal Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 486 | 293 |
|
Connective Tissue Disorders Panel PreventionGenetics, part of Exact Sciences United States | 166 | 101 |
|
Vitreoretinopathy and Wagner syndrome Amplexa Genetics Amplexa Genetics A/S Denmark | 1 | 6 |
|
Familial Exudative Vitreoretinopathy and Wagner Syndrome Amplexa Genetics Amplexa Genetics A/S Denmark | 2 | 8 |
|
Wagner vitreoretinopathy Comprehensive test HNL Genomics Connective Tissue Gene Tests United States | 1 | 1 |
|
Wagner vitreoretinopathy Sequencing test HNL Genomics Connective Tissue Gene Tests United States | 1 | 1 |
|
Wagner vitreoretinopathy Deletion / Duplication test HNL Genomics Connective Tissue Gene Tests 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.