Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Integrated Genetics Westborough LabCorp United States | 172 | 350 |
|
Integrated Genetics Westborough LabCorp United States | 287 | 578 |
|
Inheritest High Frequency panel Integrated Genetics Westborough LabCorp United States | 109 | 110 |
|
RARS2. Complete sequencing by NGS Laboratorio de Genetica Clinica SL Spain | 1 | 1 |
|
HEREDITARY ATAXIAS EXOME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 1202 |
|
EARLY INFANTILE EPILEPTIC ENCEPHALOPATHY EXOME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 139 |
|
Laboratorio de Genetica Clinica SL Spain | 1 | 696 |
|
Laboratorio de Genetica Clinica SL Spain | 1 | 245 |
|
MITOCHONDRIAL DISEASES PANEL (NUCLEAR GENES) Laboratorio de Genetica Clinica SL Spain | 1 | 1372 |
|
Clinical Biochemical Genetics Diagnostic Laboratory University Of Miami Miller School Of Medicine United States | 1 | 695 |
|
Arthrogryposis panel. NGS panel of 69 genes. Genologica Medica Spain | 135 | 69 |
|
Microcephaly and cerebellar hypoplasia panel. 48-gene NGS panel. Genologica Medica Spain | 63 | 48 |
|
Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
|
Mitochondrial genome sequencing Molecular Vision Laboratory United States | 525 | 339 |
|
Congenital Hypotonia Xpanded Panel GeneDx United States | 10 | 1423 |
|
Natera, Inc. United States | 244 | 254 |
|
Prenatal Known Familial Mutation GeneDx United States | 1 | 1716 |
|
Custom XomeDxSlice (2-150 Genes, Proband Only) GeneDx United States | 1 | 1718 |
|
GeneDx United States | 1 | 1040 |
|
Comprehensive Brain Malformations Panel GeneDx United States | 19 | 103 |
|
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.