Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Beckwith-Wiedemann syndrome panel Genologica Medica Spain | 20 | 10 |
|
Beckwith-Wiedemann syndrome panel. NGS panel of 10 genes. Genologica Medica Spain | 20 | 10 |
|
Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
|
qGenEx Intellectual disability Quantitative Genomic Medicine Laboratories, SL Spain | 3 | 1969 |
|
Fulgent Genetics United States | 5128 | 4672 |
|
High-Resolution Rapid Microarray (CGH and SNP) Allele Diagnostics United States | 247 | 231 |
|
Rapid microarray (CGH and SNP) Allele Diagnostics United States | 247 | 231 |
|
Genomic Unity® Hearing Loss Disorders Analysis Variantyx, Inc. United States | 1 | 318 |
|
Centogene AG - the Rare Disease Company Germany | 203 | 194 |
|
Centogene AG - the Rare Disease Company Germany | 829 | 848 |
|
PathGroup United States | 73 | 505 |
|
Invitae Skeletal Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 624 | 349 |
|
PreventionGenetics, part of Exact Sciences United States | 48 | 28 |
|
Baylor Genetics United States | 1 | 354 |
|
Macrosomic syndromes (WES based NGS panel of 35 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 35 |
|
Skeletal Dysplasias and Disorders Panel CGC Genetics Unilabs Portugal | 1 | 606 |
|
Inherited Loss of Hearing Panel Dhiti Omics Technologies Private Ltd India | 8 | 179 |
|
Beckwith-Wiedemann syndrome: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 1 | 2 |
|
Congenital Hypotonia Xpanded Panel GeneDx United States | 10 | 1423 |
|
Prenatal Known Familial Mutation GeneDx United States | 1 | 1716 |
|
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.