Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Genomic Unity® Renal Disorders Analysis Variantyx, Inc. United States | 1 | 425 |
|
Malformations of cortical development panel CGC Genetics Unilabs Portugal | 5 | 111 |
|
Syndromes with short stature (WES based NGS panel of 104 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 104 |
|
CGC Genetics Unilabs Portugal | 1 | 334 |
|
Mendelics Brazil | 1 | 81 |
|
Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
|
Congenital Hypotonia Xpanded Panel GeneDx United States | 10 | 1423 |
|
GeneDx United States | 2 | 2592 |
|
GeneDx United States | 1 | 1501 |
|
Galloway-Mowat syndrome: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 8 | 8 |
|
Comprehensive Glomerular Proteinuria NGS Panel Fulgent Genetics United States | 182 | 76 |
|
Fulgent Genetics United States | 1 | 1 |
|
Nephrotic Syndrome and Focal and Segmental Glomerulosclerosis Hildebrandt Laboratory Boston Children's Hospital United States | 2 | 61 |
|
Nephrotic Syndrome and Focal Segmental Glomerulosclerosis panel Clinical Genomics Laboratory Washington University in St. Louis United States | 10 | 52 |
|
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