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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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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Detection of ITD and TKD mutations on FLT3 gene CGC Genetics Unilabs Portugal | 2 | 1 |
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Centogene AG - the Rare Disease Company Germany | 323 | 329 |
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Invitae Inborn Errors of Immunity and Cytopenias Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 754 | 562 |
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Invitae Nuclear Mitochondrial Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 394 | 319 |
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Mayo Clinic Laboratories Mayo Clinic United States | 3 | 4 |
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Invitae Cerebral Palsy Spectrum Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 638 | 419 |
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Invitae Primary Immunodeficiency Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 552 | 424 |
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Labcorp Genetics (formerly Invitae) LabCorp United States | 466 | 297 |
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Inherited Metabolic Disorders Panel Dhiti Omics Technologies Private Ltd India | 376 | 317 |
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Encephalopathy, acute, infection-induced: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 8 | 8 |
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Acute Necrotizing Encephalopathy Type 1 (RANBP2 Single Gene Test) Fulgent Genetics United States | 1 | 1 |
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Comprehensive Primary Immunodeficiency NGS Panel Fulgent Genetics United States | 1048 | 472 |
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ENCEPHALOPATHY, NECROTIZING, FAMILIAL ACUTE Laboratorio de Genetica Clinica SL Spain | 1 | 1 |
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Susceptibility to Infection-Induced Acute Encephalopathy 3: gene sequencing CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 1 | 1 |
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MGZ Medical Genetics Center Germany | 1 | 1 |
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Familial acute necrotizing encephalopathy Bioarray Spain | 1 | 1 |
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RANBP2 Common Mutations 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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Fulgent Genetics United States | 1 | 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.