Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Bcell/Antibody Deficiency GenePanel Mayo Clinic Laboratories Mayo Clinic United States | 79 | 61 |
|
BLNK Gene Agammaglobulinemia type 4, autosomal recessive NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
BLNK - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 323 | 329 |
|
Centogene AG - the Rare Disease Company Germany | 829 | 848 |
|
Invitae Inborn Errors of Immunity and Cytopenias Panel Invitae United States | 755 | 562 |
|
Hematologic Cancer Fusion Analysis Institute for Genomic Medicine (IGM) Clinical Laboratory Nationwide Children's Hospital United States | 1 | 147 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Primary Antibody Deficiency Panel PreventionGenetics, part of Exact Sciences United States | 50 | 46 |
|
PreventionGenetics, part of Exact Sciences United States | 12 | 13 |
|
Invitae Primary Immunodeficiency Panel Invitae United States | 552 | 424 |
|
Invitae Agammaglobulinemia Panel Invitae United States | 39 | 36 |
|
CGC Genetics Unilabs Portugal | 1 | 385 |
|
Neonatal Baby Cheek Screening Test Mendelics Brazil | 1 | 342 |
|
Primary Immunodeficiencies Panel Mendelics Brazil | 1 | 59 |
|
Immunodeficiencies and Immunologic Diseases Panel (Complete) Mendelics Brazil | 1 | 397 |
|
Mendelics Brazil | 1 | 369 |
|
Duzen Laboratories Duzen BBAGUAS Turkey | 1 | 81 |
|
Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
|
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.