Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Primary ciliary dyskinesia (WES-based NGS panel of 34 genes, including analysis of CNVs) CGC Genetics Unilabs Portugal | 1 | 34 |
|
Congenital Heart Defects Panel CGC Genetics Unilabs Portugal | 1 | 208 |
|
CGC Genetics Unilabs Portugal | 1 | 385 |
|
CGC Genetics Unilabs Portugal | 1 | 107 |
|
Ciliary dyskinesia, primary 6 (sequence analysis of NME8 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Immunodeficiencies and Immunologic Diseases Panel (Complete) Mendelics Brazil | 1 | 397 |
|
Primary Ciliary Dyskinesia Panel Mendelics Brazil | 1 | 35 |
|
GLOBAL CILIOPATHIES EXOME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 273 |
|
SUDDEN DEATH/ IDIOPATHIC VENTRICULAR FIBRILLATION EXOME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 394 |
|
Clinical Biochemical Genetics Diagnostic Laboratory University Of Miami Miller School Of Medicine United States | 1 | 695 |
|
HETEROTAXY & SITUS INVERSUS EXOME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 41 |
|
Complete panel of pulmonology. NGS panel of 66 genes. Genologica Medica Spain | 115 | 66 |
|
Bronchiectasis panel. NGS panel of 15 genes. Genologica Medica Spain | 19 | 15 |
|
Plugin system clutter panel. NGS panel of 75 genes. Genologica Medica Spain | 76 | 75 |
|
Ciliary dyskinesia and heterotaxia. NGS panel of 40 genes. Genologica Medica Spain | 49 | 40 |
|
Primary ciliary dyskinesia panel. 36-gene NGS panel. Genologica Medica Spain | 46 | 35 |
|
Heterotaxy & Situs Inversus Panel, Sequencing ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States | 7 | 36 |
|
Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
|
NME8 Deletion/duplication analysis Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 1 | 1 |
|
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.