Clinical and research tests for C3468041 - Genetic Testing Registry (GTR)

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Results: 41 to 60 of 126

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Fanconi Anemia Panel PreventionGenetics, part of Exact Sciences United States	20	22	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Chromosomes, DEB Assay for Fanconi Anemia Quest Diagnostics Nichols Institute Chantilly United States	15	15	B Chromosome breakage studies
Chromosome DEB Assay for Fanconi anemia, Prenatal Quest Diagnostics Nichols Institute Chantilly United States	15	15	B Chromosome breakage studies
FANCONI ANEMIA, TYPE C BioReference Health United States	1	1	T Targeted variant analysis
Inheritest Custom 1;13 Genes MNG Laboratories (Medical Neurogenetics, LLC.) United States	12	12	C Sequence analysis of the entire coding region
Limb malformation panel. NGS panel of 45 genes. Genologica Medica Spain	77	45	C Sequence analysis of the entire coding region
Bone marrow failure syndrome panel. NGS panel of 122 genes. Genologica Medica Spain	194	122	C Sequence analysis of the entire coding region
Fanconi anemia panel Genologica Medica Spain	35	22	C Sequence analysis of the entire coding region
Hereditary pancreatic cancer panel. NGS panel of 22 genes. Genologica Medica Spain	61	22	C Sequence analysis of the entire coding region
Gastrointestinal atresia panel. NGS panel of 13 genes. Genologica Medica Spain	19	13	C Sequence analysis of the entire coding region
VistaSeq Comprehensive Cancer Panel Molecular Diagnostic Laboratory LabCorp United States	47	59	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Common Carrier Screening Panel HNL Genomics Connective Tissue Gene Tests United States	18	18	C Sequence analysis of the entire coding region T Targeted variant analysis
Extended Carrier Screening HNL Genomics Connective Tissue Gene Tests United States	44	45	C Sequence analysis of the entire coding region T Targeted variant analysis
Horizon 137 Male Natera, Inc. United States	130	133	E Sequence analysis of select exons C Sequence analysis of the entire coding region
Horizon 274 Male Natera, Inc. United States	244	254	E Sequence analysis of select exons C Sequence analysis of the entire coding region
FANCC Gene Sequencing by Massively Parallel Sequencing (BCM-NGSSM) Baylor Genetics United States	1	1	E Sequence analysis of select exons
FANCC Sequence Analysis (Familial Mutation/Variant Analysis) Baylor Genetics United States	1	1	T Targeted variant analysis
FANCC Prenatal Sequence Analysis (GeneAware) (Prenatal Sequence Analysis) Baylor Genetics United States	1	1	E Sequence analysis of select exons
Super Panel Plus NxGen MDx United States	116	117	D Deletion/duplication analysis E Sequence analysis of select exons C Sequence analysis of the entire coding region T Targeted variant analysis
Universal Panel Plus NxGen MDx United States	21	22	D Deletion/duplication analysis E Sequence analysis of select exons C Sequence analysis of the entire coding region T Targeted variant analysis

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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.

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Results: 41 to 60 of 126

Results: 41 to 60 of 126