Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Invitae Mendelian Disorders with Psychiatric Symptoms Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 254 | 166 |
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Invitae NIPS for Singleton Pregnancies (chromosomes 13, 18, 21) Labcorp Genetics (formerly Invitae) LabCorp United States | 11 | 11 |
|
PreventionGenetics, part of Exact Sciences United States | 177 | 161 |
|
Hereditary Hearing Loss and Deafness Panel PreventionGenetics, part of Exact Sciences United States | 362 | 227 |
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Genetics Service Unit BRIC-National Institute of Biomedical Genomics India | 1 | 1 |
|
Ambry Genetics United States | 236 | 167 |
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Ambry Genetics United States | 189 | 92 |
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Proximal 22Q Gene deletion/duplication Molecular Diagnostics Children's Hospital of Wisconsin United States | 2 | 2 |
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Invitae Autoinflammatory and Autoimmunity Syndromes Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 226 | 154 |
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Labcorp Genetics (formerly Invitae) LabCorp United States | 186 | 130 |
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Invitae Primary Immunodeficiency Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 603 | 446 |
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22q11.2 Deletion/Duplication Analysis Children's Hospital of Los Angeles, Center for Personalized Medicine United States | 5 | 1 |
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Quest Diagnostics Nichols Institute San Juan Capistrano United States | 14 | 12 |
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Invitae Congenital Heart Disease Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 118 | 55 |
|
FISH, DiGeorge, Velocardio Facial Syndrome (VCFS) Quest Diagnostics Nichols Institute San Juan Capistrano United States | 2 | 1 |
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FISH, DiGeorge, Velocardio Facial Syndrome (VCFS) Quest Diagnostics Nichols Institute Chantilly United States | 2 | 1 |
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UW Cytogenetic Services Wisconsin State Laboratory of Hygiene United States | 2 | 1 |
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GeneSeq® Cardio Single Gene Analysis Integrated Genetics Westborough LabCorp United States | 55 | 177 |
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Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 4 | 1 |
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Comprehensive Hearing Loss + mtDNA MNG Laboratories (Medical Neurogenetics, LLC.) United States | 218 | 300 |
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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.