Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Integrated Genetics Westborough LabCorp United States | 287 | 578 |
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Primary Immunodeficiencies Panel Mendelics Brazil | 1 | 59 |
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Immunodeficiencies and Immunologic Diseases Panel (Complete) Mendelics Brazil | 1 | 397 |
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Mendelics Brazil | 1 | 369 |
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Bare lymphocyte syndrome: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 5 | 6 |
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Severe Combined Immunodeficiency Asper Biogene Asper Biogene LLC Estonia | 61 | 43 |
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Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
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Prenatal Known Familial Mutation GeneDx United States | 1 | 1716 |
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Custom XomeDxSlice (2-150 Genes, Proband Only) GeneDx United States | 1 | 1718 |
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Very Early Onset Inflammatory Bowel Disease (VEO-IBD) Panel Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 1 | 97 |
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Comprehensive Primary Immunodeficiency NGS Panel Fulgent Genetics United States | 1048 | 472 |
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B-Positive Severe Combined Immunodeficiency NGS Panel Fulgent Genetics United States | 38 | 26 |
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Severe Combined Immunodeficiency NGS Panel Fulgent Genetics United States | 330 | 90 |
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IMMUNODEFICIENCY BY DEFECTIVE EXPRESSION OF HLA CLASS 2 (BARE LYMPHOCYTE SYNDROME TYPE 2) Laboratorio de Genetica Clinica SL Spain | 1 | 4 |
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Severe Combined Immunodeficiency Panel Blueprint Genetics Finland | 1 | 79 |
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Primary Immunodeficiency Panel Blueprint Genetics Finland | 2 | 275 |
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Combined immunodeficiencies Panel CeGaT GmbH Germany | 23 | 60 |
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Bare lymphocyte syndrome type 2 Bioarray Spain | 1 | 1 |
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RFX5 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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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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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.