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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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Labcorp Genetics (formerly Invitae) LabCorp United States | 24 | 8 |
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F2 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 4 | 1 |
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Stroke, Cerebral Hemorrhage, Hemiplegia, and Migraine Panel PreventionGenetics, part of Exact Sciences United States | 346 | 160 |
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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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Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins University, School of Medicine United States | 525 | 338 |
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IBC Instituto de Bioquimica Clinica SRL Argentina | 3 | 1 |
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IBC Instituto de Bioquimica Clinica SRL Argentina | 3 | 1 |
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Invitae Hereditary Thrombophilia Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 24 | 11 |
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Baylor Genetics United States | 11 | 3 |
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Baylor Genetics United States | 4 | 1 |
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Clotting factor deficiency panel. 16-gene NGS panel. Genologica Medica Spain | 29 | 16 |
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Bleeding disorder / coagulopathy panel. NGS panel of 62 genes. Genologica Medica Spain | 96 | 62 |
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Asper Biogene Asper Biogene LLC Estonia | 85 | 64 |
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Factor II (Prothrombin) G20210A Genotyping and MTHFR C677T and A1298C Genotyping PathGroup United States | 5 | 2 |
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Factor II (Prothrombin) G20210A Genotyping and SERPINE1 (PAI-1) 4G/5G Genotyping PathGroup United States | 4 | 2 |
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Fulgent Genetics United States | 46 | 18 |
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Comprehensive Thrombosis, Platelet Disorder, and Coagulation Deficiency NGS Panel Fulgent Genetics United States | 146 | 82 |
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Beacon Expanded Female Carrier Screening Plus Panel Fulgent Genetics United States | 716 | 335 |
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