Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Chromosomes, DEB Assay for Fanconi Anemia Quest Diagnostics Nichols Institute Chantilly United States | 15 | 15 |
|
Chromosome DEB Assay for Fanconi anemia, Prenatal Quest Diagnostics Nichols Institute Chantilly United States | 15 | 15 |
|
Limb malformation panel. NGS panel of 45 genes. Genologica Medica Spain | 77 | 45 |
|
Bone marrow failure syndrome panel. NGS panel of 122 genes. Genologica Medica Spain | 194 | 122 |
|
Genologica Medica Spain | 35 | 22 |
|
CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 64 | 39 |
|
CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 95 | 62 |
|
Fulgent Genetics United States | 180 | 60 |
|
Comprehensive Primary Immunodeficiency NGS Panel Fulgent Genetics United States | 1048 | 472 |
|
Fanconi Anemia: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 21 | 21 |
|
Bone Marrow Failure Related Disorders , Panel Massive Sequencing (NGS) 59 Genes Reference Laboratory Genetics Spain | 63 | 58 |
|
Oncology Genetic Panel , Panel Massive Sequencing (NGS) 90 Genes Reference Laboratory Genetics Spain | 126 | 90 |
|
Fanconi Anemia , Panel Massive Sequencing (NGS) 15 Genes Reference Laboratory Genetics Spain | 15 | 15 |
|
Asper Biogene Asper Biogene LLC Estonia | 17 | 17 |
|
Full Comprehensive Cancer Panel Fulgent Genetics United States | 329 | 127 |
|
GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Spain | 67 | 80 |
|
GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Spain | 14 | 16 |
|
Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center Netherlands | 1 | 1 |
|
CeGaT GmbH Germany | 17 | 16 |
|
FANCI Deletion/duplication analysis Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 1 | 1 |
|
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.