Filters
Results: 1 to 20 of 20
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics United States | 287 | 218 |
|
Genomic Unity® Hearing Loss Disorders Analysis Variantyx, Inc. United States | 1 | 318 |
|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
Invitae Connective Tissue Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 195 | 92 |
|
PreventionGenetics, part of Exact Sciences United States | 285 | 137 |
|
Invitae Comprehensive Deafness Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 405 | 219 |
|
Invitae Skeletal Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 624 | 349 |
|
Invitae Stickler Syndrome Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 32 | 9 |
|
Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins University, School of Medicine United States | 33 | 10 |
|
Connective Tissue Disorders Panel PreventionGenetics, part of Exact Sciences United States | 166 | 101 |
|
HNL Genomics Connective Tissue Gene Tests United States | 8 | 8 |
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Stickler syndrome Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 8 | 8 |
|
Stickler syndrome Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 8 | 8 |
|
PreventionGenetics, part of Exact Sciences United States | 30 | 12 |
|
Baylor Genetics United States | 1 | 354 |
|
Connective Tissue Disorders Panel Baylor Genetics United States | 1 | 92 |
|
Deafness or hypoacusis panel_v.2.0 CGC Genetics Unilabs Portugal | 1 | 272 |
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Myopia 28, autosomal recessive (deletion/duplication analysis of LOXL3) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 39 | 13 |
|
Fulgent Genetics United States | 1 | 1 |
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Results: 1 to 20 of 20
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.