Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Somatic Overgrowth and Vascular Malformations Gene Panel Genetic Diagnostic Laboratory University of Pennsylvania School of Medicine United States | 9 | 34 |
|
PreventionGenetics, part of Exact Sciences United States | 15 | 14 |
|
Milroy Disease (Lymphedema Type I) via the FLT4 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
Vascular Malformations Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States | 24 | 28 |
|
Vascular Anomalies Panel with interpretation Clinical Genomics Laboratory Washington University in St. Louis United States | 1 | 65 |
|
Laboratory for Molecular Pediatric Pathology Boston Children's Hospital United States | 1 | 35 |
|
Comprehensive Solid Tumor Panel Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 2 | 316 |
|
Lymphedema hereditary (WES based NGS panel of 22 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 22 |
|
Congenital Heart Defects Panel CGC Genetics Unilabs Portugal | 1 | 208 |
|
CGC Genetics Unilabs Portugal | 1 | 277 |
|
Fetal hydrops (WES based NGS panel for 66 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 66 |
|
Milroy disease (sequence analysis of FLT4 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Milroy disease (sequence analysis of exons 17-26 of FLT4 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
OnkoSight Advanced Comprehensive Solid Tumor Panel (DNA/RNA) BioReference Health United States | 1 | 523 |
|
OnkoSight Advanced 523 Gene NGS Panel BioReference Health United States | 1 | 523 |
|
Caris Life Sciences United States | 1 | 591 |
|
OncoAlly™ Solid Tumor Analysis Variantyx, Inc. United States | 1 | 433 |
|
Quest Diagnostics Nichols Institute San Juan Capistrano United States | 1 | 523 |
|
Lymphatic malformations and related disorders panel. NGS panel of 11 genes. Genologica Medica Spain | 31 | 11 |
|
Congenital heart defects: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 10 | 10 |
|
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.