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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
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Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
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Centogene AG - the Rare Disease Company Germany | 325 | 316 |
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Invitae Rhabdomyolysis and Metabolic Myopathy Panel Invitae United States | 202 | 128 |
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Myofibrillar myopathy and related disorders Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 19 | 11 |
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Myofibrillar myopathy and related disorders Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 19 | 11 |
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Invitae United States | 409 | 164 |
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Invitae United States | 208 | 81 |
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Invitae Comprehensive Carrier Screen Invitae United States | 886 | 547 |
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Myofibrillar myopathy and related disorders Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 19 | 11 |
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Myofibrillar myopathy and related disorders Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 19 | 11 |
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Comprehensive Neuromuscular Panel PreventionGenetics, part of Exact Sciences United States | 183 | 142 |
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Invitae Comprehensive Muscular Dystrophy Panel Invitae United States | 114 | 52 |
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Invitae Comprehensive Myopathy Panel Invitae United States | 143 | 70 |
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Invitae Comprehensive Neuromuscular Disorders Panel Invitae United States | 353 | 208 |
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Invitae Cardiomyopathy Comprehensive Panel Invitae United States | 198 | 82 |
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Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel Invitae United States | 239 | 100 |
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Invitae Hypertrophic Cardiomyopathy Panel Invitae United States | 69 | 30 |
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X-chromosome High Resolution microarray analysis Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center United States | 240 | 171 |
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FHL1-Myopathies via the FHL1 Gene PreventionGenetics, part of Exact Sciences United States | 4 | 1 |
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FHL1 Deletion/duplication analysis Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 5 | 1 |
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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.