Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Center for Genetics at Saint Francis Saint Francis Hospital United States | 2 | 1 |
|
GJB6-Related DFNB 1 Nonsyndromic Hearing Loss and Deafness Molecular Genetics Laboratory London Health Sciences Centre Canada | 1 | 2 |
|
GJB2-Related DFNB 1 Nonsyndromic Hearing Loss and Deafness Molecular Genetics Laboratory London Health Sciences Centre Canada | 1 | 2 |
|
Carrier Screening - Comprehensive Panel (145 Genes) Genesys Diagnostics Genesys Diagnostics, Inc. United States | 185 | 145 |
|
GJB2 Gene Deafness with keratopachydermia and constrictions of fingers and toes NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
GJB2 Gene Deafness, autosomal dominant type 3A NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
GJB2 Gene Deafness, autosomal recessive type 1A NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
GJB2 Gene Keratitis ichthyosis deafness syndrome autosomal dominant NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
GJB2 Gene Keratoderma, palmoplantar, with deafness NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
GJB2 Gene Knuckle pads and leukonychia sensorineural deafness NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics United States | 287 | 218 |
|
Sensorineural hearing loss, connexin 26 and 30 (GJB2 and GJB6 genes) Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS Chile | 1 | 2 |
|
GeneID Lab - Advanced Molecular Diagnostics United States | 73 | 61 |
|
Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel Otogenetics United States | 122 | 128 |
|
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 |
|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
Centogene AG - the Rare Disease Company Germany | 316 | 314 |
|
GJB2 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 7 | 1 |
|
Carrier Screening Guidelines-Based Panel Ambry Genetics United States | 199 | 164 |
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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.