Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Hypomagnesemia (WES based NGS panel of 17 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 17 |
|
Renal calcifications (nephrocalcinosis) (NGS panel of 36 genes, including CNV analysis)) CGC Genetics Unilabs Portugal | 1 | 36 |
|
CGC Genetics Unilabs Portugal | 1 | 334 |
|
Hypomagnesemia type 1 (deletion/duplication analysis of TRPM6 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Hypomagnesemia type 1 (sequence analysis of TRPM6 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Neonatal Baby Cheek Screening Test Mendelics Brazil | 1 | 342 |
|
Kidney Function Disorders Panel Mendelics Brazil | 1 | 23 |
|
Mendelics Brazil | 1 | 369 |
|
TRPM6. Complete sequencing by NGS Laboratorio de Genetica Clinica SL Spain | 1 | 1 |
|
Laboratorio de Genetica Clinica SL Spain | 1 | 696 |
|
MITOCHONDRIAL DISEASES PANEL (NUCLEAR GENES) Laboratorio de Genetica Clinica SL Spain | 1 | 1372 |
|
Hypomagnesemia panel. NGS panel of 19 genes. Genologica Medica Spain | 27 | 19 |
|
Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
|
Asper Biogene Asper Biogene LLC Estonia | 27 | 18 |
|
GeneDx United States | 2 | 2592 |
|
GeneDx United States | 1 | 1501 |
|
NewbornDx Advanced Sequencing Evaluation Athena Diagnostics United States | 1 | 1722 |
|
Hypomagnesemia: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 6 | 6 |
|
Comprehensive Metabolism NGS Panel Fulgent Genetics United States | 602 | 355 |
|
Fulgent Genetics United States | 121 | 23 |
|
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.