Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Cardiology Sequencing- Arrhythmia Comprehensive Panel (134 Genes) Genesys Diagnostics Genesys Diagnostics, Inc. United States | 88 | 134 |
|
Cardiology Sequencing- Full Panel (174 Genes) Genesys Diagnostics Genesys Diagnostics, Inc. United States | 122 | 174 |
|
EYA4 Gene Deafness, autosomal dominant type 10 NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
EYA4 Gene Cardiomyopathy, dilated type 1J NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
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 |
|
Cardiomyopathies General Panel Health in Code Spain | 1 | 173 |
|
Congenital heart diseases Panel Health in Code Spain | 1 | 76 |
|
Health in Code Spain | 1 | 218 |
|
Health in Code Spain | 1 | 39 |
|
Cardiovascular Diseases_General Panel Health in Code Spain | 1 | 380 |
|
Congenital Heart Diseases Panel Health in Code Spain | 1 | 39 |
|
Health in Code Spain | 1 | 149 |
|
Health in Code Spain | 1 | 81 |
|
Inherited Cardiovascular Diseases and Sudden Death Panel Health in Code Spain | 1 | 213 |
|
Genomic Unity® Hearing Loss Disorders Analysis Variantyx, Inc. United States | 1 | 318 |
|
AudioloGene Hearing Loss Panel Mayo Clinic Laboratories Mayo Clinic United States | 1 | 200 |
|
EYA4 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 289 | 275 |
|
Centogene AG - the Rare Disease Company Germany | 203 | 194 |
|
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.