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Other countries
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
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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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Lysosomal and peroxisomal diseases (WES based NGS panel of 122 genes, including analysis of CNVs) CGC Genetics Unilabs Portugal | 1 | 122 |
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Pan Cardiomyopathy Panel (62 Genes) Laboratory for Molecular Medicine Mass General Brigham Personalized Medicine United States | 100 | 61 |
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TPM1 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
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Labcorp Genetics (formerly Invitae) LabCorp United States | 409 | 164 |
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Labcorp Genetics (formerly Invitae) LabCorp United States | 208 | 81 |
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Invitae 78 Gene Actionable Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 220 | 75 |
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Ambry Genetics United States | 58 | 30 |
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Ambry Genetics United States | 58 | 30 |
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Ambry Genetics United States | 100 | 37 |
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Ambry Genetics United States | 236 | 167 |
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Ambry Genetics United States | 138 | 56 |
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Ambry Genetics United States | 189 | 92 |
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PreventionGenetics, part of Exact Sciences United States | 112 | 111 |
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PreventionGenetics, part of Exact Sciences United States | 66 | 66 |
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PreventionGenetics, part of Exact Sciences United States | 63 | 49 |
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Comprehensive Cardiology Panel PreventionGenetics, part of Exact Sciences United States | 224 | 202 |
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Invitae Dilated Cardiomyopathy and Left Ventricular Noncompaction Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 134 | 54 |
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Invitae Cardiomyopathy Comprehensive Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 198 | 82 |
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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.