Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Sarcoma Comprehensive NGS Fusion Panel NeoGenomics Laboratories NeoGenomics Laboratories, Inc. United States | 1 | 97 |
|
Non-Ewing Sarcoma NGS Fusion Profile NeoGenomics Laboratories NeoGenomics Laboratories, Inc. United States | 4 | 24 |
|
GeneDx United States | 1 | 877 |
|
Dystonia and Parkinsonism Panel GeneDx United States | 20 | 73 |
|
GeneDx United States | 2 | 2592 |
|
GeneDx United States | 1 | 999 |
|
GeneDx United States | 1 | 1501 |
|
Paired Tumor/Normal - Comprehensive Solid Tumor Panel Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 2 | 315 |
|
Basal ganglia calcification, idiopathic: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 5 | 5 |
|
Basal Ganglia Calcification NGS Panel Fulgent Genetics United States | 4 | 2 |
|
Blueprint Genetics Finland | 1 | 20 |
|
Caris MI TumorSeek Comprehensive Genomic Profile Caris Life Sciences United States | 1 | 591 |
|
Primary Familial Brain Calcification: gene deletion/duplication panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 1 | 2 |
|
Primary Familial Brain Calcification: gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 1 | 4 |
|
Familial Meningioma , Panel Massive Sequencing (NGS) 6 Genes Reference Laboratory Genetics Spain | 1 | 6 |
|
Schwannomatosis, Panel Massive Sequencing (NGS) 7 Genes Reference Laboratory Genetics Spain | 3 | 7 |
|
Fahr Disease , Panel massive Sequencing (NGS) (SLC20A2, PDGFRB, PDGFB) Genes Reference Laboratory Genetics Spain | 3 | 3 |
|
BILATERAL STRIOPALLIDODENTATE CALCINOSIS (BSPDC) Laboratorio de Genetica Clinica SL Spain | 4 | 4 |
|
Blueprint Genetics Finland | 1 | 22 |
|
Neurogenetic Disorders - panels MGZ Medical Genetics Center Germany | 14 | 597 |
|
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.