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New filters have been added to narrow your search: Test target, to filter by number of genes; Genes and Conditions, to search by gene symbol or condition name; and Labs, to search by a laboratory name.
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Labs matching your search
30 labs with tests matching your search
Results:
95 genetic tests from 30 labs with tests matching your search
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods | |
|---|---|---|---|---|
| 1 | 1 |
| ||
| 1 | 1 |
| ||
| 1 | 1 |
| ||
| 469 | 448 |
| ||
| 1 | 1 |
| ||
| 182 | 117 |
| ||
| 79 | 61 |
| ||
| 34 | 26 |
| ||
ADA2 Gene Polyarteritis nodosa, childhood-onset NGS Genetic DNA Test | 1 | 1 |
| |
| 1 | 1 |
| ||
| 23 | 30 |
| ||
| 23 | 32 |
| ||
Multigene panel for cerebral small vessel diseases based on whole-exome sequencing | 1 | 18 |
| |
Multigene panel for leukodystrophies and leukoencephalopathies based on whole-exome sequencing | 2 | 115 |
| |
Multigene panel for autoinflammatory syndromes based on whole-exome sequencing | 1 | 101 |
| |
Multigene panel for primary immunodeficiencies based on whole-exome sequencing | 1 | 535 |
| |
| 374 | 386 |
| ||
| 693 | 388 |
| ||
| 56 | 69 |
| ||
| 754 | 562 |
|
95 tests from 30 labs
Page 1 of 5❯CECR1 by MGZ Medical Genetics Center
1 condition, 1 gene
1 condition, 1 gene
CECR1 Gene Sequencing by Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory, Cincinnati Children's Hospital Medical Center
1 condition, 1 gene
1 condition, 1 gene
Adenosine deaminase 2 deficiency (ADA2 gene) by Amsterdam UMC, Location AMC, Laboratory Genetic Metabolic Diseases, LGMD
1 condition, 1 gene
1 condition, 1 gene
RenaDx™: Comprehensive Renal Disease Genetics Panel by Precision Medicine Care (PMC®)
469 conditions, 448 genes
469 conditions, 448 genes
Deficiency of ADA2 by Inflammatory Disease Section/Clinical Genetics Service, National Human Genome Research Institute
1 condition, 1 gene
1 condition, 1 gene
Autoinflammatory Gene Panel by Mayo Clinic Laboratories, Mayo Clinic
182 conditions, 117 genes
182 conditions, 117 genes
Bcell/Antibody Deficiency GenePanel by Mayo Clinic Laboratories, Mayo Clinic
79 conditions, 61 genes
79 conditions, 61 genes
ALPS Gene Panel by Mayo Clinic Laboratories, Mayo Clinic
34 conditions, 26 genes
34 conditions, 26 genes
ADA2 Gene Sneddon syndrome NGS Genetic DNA Test by DNA Labs India
1 condition, 1 gene
1 condition, 1 gene
Cerebrovascular Gene Panel by Mayo Clinic Laboratories, Mayo Clinic
23 conditions, 30 genes
23 conditions, 30 genes
NGS Panel for Diamond-Blackfan Anemia by BloodGenetics
23 conditions, 32 genes
23 conditions, 32 genes
Multigene panel for cerebral small vessel diseases based on whole-exome sequencing by CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
1 condition, 18 genes
1 condition, 18 genes
Multigene panel for leukodystrophies and leukoencephalopathies based on whole-exome sequencing by CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
2 conditions, 115 genes
2 conditions, 115 genes
Multigene panel for autoinflammatory syndromes based on whole-exome sequencing by CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
1 condition, 101 genes
1 condition, 101 genes
Multigene panel for primary immunodeficiencies based on whole-exome sequencing by CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
1 condition, 535 genes
1 condition, 535 genes
Inborn Errors of Immunity GenePanel by Mayo Clinic Laboratories, Mayo Clinic
374 conditions, 386 genes
374 conditions, 386 genes
Invitae Expanded Renal Disease Panel by Labcorp Genetics (formerly Invitae), LabCorp
693 conditions, 388 genes
693 conditions, 388 genes
NGS Panel for Bone Marrow failure by BloodGenetics
56 conditions, 69 genes
56 conditions, 69 genes
Invitae Inborn Errors of Immunity and Cytopenias Panel by Labcorp Genetics (formerly Invitae), LabCorp
754 conditions, 562 genes
754 conditions, 562 genes
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.