Filters
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.
Other countries
Labs matching your search
10 labs with tests matching your search, 1 lab matching in other ways
| Lab name | Tests matching your search |
|---|---|
| Bionano Laboratories United States | 1 |
| CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 1 |
| CHEO Genetics Diagnostic Laboratory Canada | 1 |
| Fulgent Genetics United States | 2 |
| GeneDx United States | 2 |
| MGZ Medical Genetics Center Germany | 2 |
| Molecular Diagnostics Platform_Biogipuzkoa Health Research Institute Spain | 2 |
| Quantitative Genomic Medicine Laboratories, SL Spain | 1 |
| Revvity Omics United States | 1 |
| University of Iowa Diagnostic Laboratories United States | 1 |
| Praxis Genomics United States | 0 |
Results:
14 genetic tests from 10 labs with tests matching your search, 1 lab matching in other ways
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods | |
|---|---|---|---|---|
| 1 | 1 |
| ||
| 2 | 5 |
| ||
| 2 | 5 |
| ||
| 2 | 7 |
| ||
| 1 | 1 |
| ||
| 3 | 1969 |
| ||
| 2 | 2592 |
| ||
| 1 | 1501 |
| ||
| 1 | 1 |
| ||
| 1 | 1 |
| ||
| 1 | 2 |
| ||
| 1 | 1 |
| ||
Facioscapulohumeral muscular dystrophy type 2 (FSHD2) - SMCHD1 and DNMT3B gene sequence analysis | 1 | 2 |
| |
| 1 | 1 |
|
14 tests from 10 labs
FSHD (Facioscapulohumeral muscular dystrophy) TYPE 1 by Revvity Omics, Revvity
1 condition, 1 gene
1 condition, 1 gene
Muscle Disease with FSHD Phenocopies by MGZ Medical Genetics Center
2 conditions, 5 genes
2 conditions, 5 genes
Facioscapulohumeral Muscular Dystrophy by University of Iowa Diagnostic Laboratories, University of Iowa Health Care
2 conditions, 5 genes
2 conditions, 5 genes
Facioscapulohumeral muscular dystrophy by MGZ Medical Genetics Center
2 conditions, 7 genes
2 conditions, 7 genes
Facioscapulohumeral muscular dystrophy by CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario
1 condition, 1 gene
1 condition, 1 gene
qGenEx Intellectual disability by Quantitative Genomic Medicine Laboratories, SL
3 conditions, 1969 genes
3 conditions, 1969 genes
EpiXpanded Panel by GeneDx
1 condition, 1501 genes
1 condition, 1501 genes
FRG2C Single Gene by Fulgent Genetics
1 condition, 1 gene
1 condition, 1 gene
FRG1 Single Gene by Fulgent Genetics
1 condition, 1 gene
1 condition, 1 gene
Facioscapulohumeral muscular dystrophy type 1 testing by Bionano Laboratories
1 condition, 2 genes
1 condition, 2 genes
Facioscapulohumeral muscular dystrophy type 1 (FSHD1) by Molecular Diagnostics Platform_Biogipuzkoa Health Research Institute, Biogipuzkoa Health Research Institute
1 condition, 1 gene
1 condition, 1 gene
Facioscapulohumeral muscular dystrophy type 2 (FSHD2) - SMCHD1 and DNMT3B gene sequence analysis by Molecular Diagnostics Platform_Biogipuzkoa Health Research Institute, Biogipuzkoa Health Research Institute
1 condition, 2 genes
1 condition, 2 genes
Facioscapulohumeral Muscular Dystrophy: gene sequencing by CEN4GEN Institute for Genomics and Molecular Diagnostics
1 condition, 1 gene
1 condition, 1 gene
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.