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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Pan Cardiomyopathy Panel (62 Genes) Laboratory for Molecular Medicine Mass General Brigham Personalized Medicine United States | 101 | 61 |
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Centogene US, LLC - The Rare Disease Company United States | 289 | 275 |
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MYOZ2 - NGS including CNV analysis Centogene US, LLC - The Rare Disease Company United States | 1 | 1 |
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MYOZ2 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
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Centogene AG - the Rare Disease Company Germany | 289 | 275 |
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Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
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Ambry Genetics United States | 59 | 30 |
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Ambry Genetics United States | 59 | 30 |
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Ambry Genetics United States | 237 | 167 |
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Ambry Genetics United States | 139 | 56 |
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Ambry Genetics United States | 190 | 92 |
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PreventionGenetics United States | 113 | 106 |
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Hypertrophic Cardiomyopathy Panel PreventionGenetics United States | 61 | 56 |
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Comprehensive Cardiology Panel PreventionGenetics United States | 220 | 196 |
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MYOZ2 Deletion/duplication analysis Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 1 | 1 |
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Sudden death (WES based NGS panel of 83 genes, including CNV analysis) Unilabs Genetics CGC Genetics Portugal | 172 | 80 |
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Hypertrophic cardiomyopathy (WES based NGS panel of 68 genes, including CNV analysis) Unilabs Genetics CGC Genetics Portugal | 150 | 68 |
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Unilabs Genetics CGC Genetics Portugal | 268 | 140 |
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Cardiomyopathy, familial hypertrophic 16 (sequence analysis of MYOZ2 gene) Unilabs Genetics CGC Genetics Portugal | 1 | 1 |
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Arrhythmia & Cardiomyopathy Panel, Comprehensive CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 212 | 93 |
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