Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Fulgent Genetics United States | 21 | 12 |
|
Baylor Genetics United States | 842 | 637 |
|
Deafness, autosomal dominant 11 MedGene Slovakia | 1 | 1 |
|
Comprehensive Eye Disorders NGS Panel Fulgent Genetics United States | 1018 | 459 |
|
Fulgent Genetics United States | 141 | 97 |
|
Deafness, autosomal dominant 11 Praxis fuer Humangenetik Wien Austria | 1 | 1 |
|
Usher Syndrome Panel by next-generation sequencing Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 18 | 9 |
|
Hereditary Hearing Loss-Common and Non-Syndromic Hearing Loss Panel Genome Diagnostics Laboratory Hospital For Sick Children Canada | 64 | 57 |
|
OtoSeq Hearing Loss Panel by next-generation sequencing (NGS) Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 36 | 23 |
|
Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 3 | 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.