Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Waardenburg Syndrome Type IVA via the EDNRB Gene PreventionGenetics, part of Exact Sciences United States | 3 | 1 |
|
Craniosynostosis panel. NGS panel of 37 genes. Genologica Medica Spain | 113 | 37 |
|
Mitochondrial genome sequencing Molecular Vision Laboratory United States | 526 | 339 |
|
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 |
|
Comprehensive Hearing Loss NGS Panel Fulgent Genetics United States | 332 | 167 |
|
Hearing Loss Advanced Sequencing and CNV Evaluation Athena Diagnostics Inc United States | 249 | 184 |
|
Waardenburg Syndrome , Panel Massive Sequencing (NGS) 6 Genes Reference Laboratory Genetics Spain | 8 | 6 |
|
WAARDENBURG-SHAH SYNDROME, NEUROLOGICAL VARIANT (TYPE 4) Laboratorio de Genetica Clinica SL Spain | 3 | 3 |
|
Waardenburg Syndrome Type 4A , Sequencing EDNRB Gene Reference Laboratory Genetics Spain | 1 | 1 |
|
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 9 | 6 |
|
Molecular Vision Laboratory United States | 19 | 7 |
|
Molecular Vision Laboratory United States | 7 | 3 |
|
Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 198 | 157 |
|
Asper Biogene Asper Biogene LLC Estonia | 9 | 7 |
|
Genetic disorders with abnormal pigmentation Panel CeGaT GmbH Germany | 29 | 32 |
|
Hermansky-Pudlak Syndrome/Oculocutaneous Albinism/Pigmentation panel Molecular Vision Laboratory United States | 45 | 29 |
|
Fulgent Genetics United States | 3 | 1 |
|
Hirschsprung Disease NGS Panel Fulgent Genetics United States | 15 | 5 |
|
Fulgent Genetics United States | 5129 | 4672 |
|
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.