Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Invitae Frontotemporal Dementia with C9orf72 Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 30 | 14 |
|
VCP - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 3 | 1 |
|
Labcorp Genetics (formerly Invitae) LabCorp United States | 72 | 33 |
|
PreventionGenetics, part of Exact Sciences United States | 27 | 19 |
|
Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Dementia (FTD) Panel PreventionGenetics, part of Exact Sciences United States | 45 | 38 |
|
Amyotrophic Lateral Sclerosis (ALS) Panel PreventionGenetics, part of Exact Sciences United States | 32 | 29 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins University, School of Medicine United States | 480 | 254 |
|
Paget disease of bone and related disorders Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 7 | 7 |
|
Paget disease of bone and related disorders NGS panel HNL Genomics Connective Tissue Gene Tests United States | 7 | 7 |
|
Paget disease of bone and related disorders Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 7 | 7 |
|
Invitae Frontotemporal Dementia Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 29 | 13 |
|
Invitae Comprehensive Myopathy Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 143 | 70 |
|
Invitae Comprehensive Neuromuscular Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 353 | 208 |
|
Institute for Human Genetics University Medical Center Freiburg Germany | 3 | 1 |
|
Amyotrophic lateral sclerosis panel. 32-gene NGS panel. Genologica Medica Spain | 66 | 32 |
|
Dementia panel. NGS panel of 21 genes. Genologica Medica Spain | 44 | 21 |
|
Comprehensive Dementia (NGS Panel and Copy Number Analysis) MNG Laboratories (Medical Neurogenetics, LLC.) United States | 10 | 145 |
|
Inclusion body myopathy / Paget disease / frontotemporal dementia: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 3 | 3 |
|
Inclusion Body Myopathy NGS Panel Fulgent Genetics United States | 21 | 5 |
|
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.