Filters
reset allTests 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 |
|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
EDN3 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
|
Congenital Anomalies of the Gastrointestinal Tract Panel PreventionGenetics, part of Exact Sciences United States | 297 | 180 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Hereditary Hearing Loss and Deafness Panel PreventionGenetics, part of Exact Sciences United States | 360 | 222 |
|
PreventionGenetics, part of Exact Sciences United States | 39 | 33 |
|
Waardenburg syndrome Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 8 | 7 |
|
Waardenburg syndrome Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 8 | 7 |
|
Waardenburg syndrome NGS panel HNL Genomics Connective Tissue Gene Tests United States | 8 | 7 |
|
PreventionGenetics, part of Exact Sciences United States | 12 | 6 |
|
Hirschsprung Disease 4 (HSCR4) via the EDN3 Gene PreventionGenetics, part of Exact Sciences United States | 3 | 1 |
|
Waardenburg Syndrome Type IVB via the EDN3 Gene PreventionGenetics, part of Exact Sciences United States | 3 | 1 |
|
Complete panel of pulmonology. NGS panel of 66 genes. Genologica Medica Spain | 115 | 66 |
|
Central hypoventilation and apnea panel. NGS panel of 15 genes. Genologica Medica Spain | 37 | 15 |
|
Mitochondrial genome sequencing Molecular Vision Laboratory United States | 526 | 339 |
|
Waardenburg Syndrome (NGS Panel and Copy Number Analysis) MNG Laboratories (Medical Neurogenetics, LLC.) United States | 10 | 7 |
|
Waardenburg syndrome: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 10 | 7 |
|
Syndromic Hearing Loss NGS Panel Fulgent Genetics United States | 223 | 83 |
|
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.