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Other countries
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
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Centogene AG - the Rare Disease Company Germany | 218 | 135 |
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Centogene AG - the Rare Disease Company Germany | 74 | 34 |
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NOTCH1 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
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Invitae Adams-Oliver Syndrome Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 9 | 8 |
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Invitae Connective Tissue Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 195 | 92 |
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Invitae Leukodystrophy and Genetic Leukoencephalopathy Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 971 | 680 |
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Congenital Anomalies of the Gastrointestinal Tract Panel PreventionGenetics, part of Exact Sciences United States | 297 | 180 |
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Invitae Limb and Digital Malformations Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 356 | 177 |
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Nonsyndromic Congenital Heart Disease Panel PreventionGenetics, part of Exact Sciences United States | 54 | 44 |
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PreventionGenetics, part of Exact Sciences United States | 7 | 8 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Connective Tissue Disorders Panel PreventionGenetics, part of Exact Sciences United States | 166 | 101 |
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Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins University, School of Medicine United States | 162 | 129 |
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Adams-Oliver syndrome Deletion / Duplication test HNL Genomics Connective Tissue Gene Tests United States | 1 | 1 |
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Adams-Oliver syndrome Comprehensive test HNL Genomics Connective Tissue Gene Tests United States | 1 | 1 |
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Adams-Oliver syndrome NGS test HNL Genomics Connective Tissue Gene Tests United States | 1 | 1 |
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Ambry Genetics United States | 50 | 35 |
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FBN1 gene sequence and deletion/duplication reflex to TAADNext® Ambry Genetics United States | 50 | 35 |
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Ambry Genetics United States | 236 | 167 |
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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.