Clinical and research tests for C3469528 - Genetic Testing Registry (GTR)

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Results: 21 to 40 of 47

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
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
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
Aplastic Anemia Panel CNH Molecular Diagnostics Laboratory Childrens National Hospital United States	64	39	C Sequence analysis of the entire coding region
Bone Marrow Failure Panel CNH Molecular Diagnostics Laboratory Childrens National Hospital United States	95	62	C Sequence analysis of the entire coding region
Bone Marrow Failure NGS Panel Fulgent Genetics United States	180	60	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Primary Immunodeficiency NGS Panel Fulgent Genetics United States	1048	472	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Fanconi Anemia: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	21	21	C Sequence analysis of the entire coding region
Bone Marrow Failure Related Disorders , Panel Massive Sequencing (NGS) 59 Genes Reference Laboratory Genetics Spain	63	58	C Sequence analysis of the entire coding region
Oncology Genetic Panel , Panel Massive Sequencing (NGS) 90 Genes Reference Laboratory Genetics Spain	126	90	C Sequence analysis of the entire coding region
Fanconi Anemia , Panel Massive Sequencing (NGS) 15 Genes Reference Laboratory Genetics Spain	15	15	C Sequence analysis of the entire coding region
Fanconi Anemia Asper Biogene Asper Biogene LLC Estonia	17	17	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Full Comprehensive Cancer Panel Fulgent Genetics United States	329	127	D Deletion/duplication analysis C Sequence analysis of the entire coding region
FANCL - Gene sequencing Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center Netherlands	1	1	E Sequence analysis of select exons T Targeted variant analysis
Fanconi anemia Panel CeGaT GmbH Germany	17	16	C Sequence analysis of the entire coding region
FANCL Deletion/duplication analysis Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States	1	1	D Deletion/duplication analysis
Cancer Predisposition Asper Biogene Asper Biogene LLC Estonia	135	98	D Deletion/duplication analysis C Sequence analysis of the entire coding region
FANCL Single Gene Fulgent Genetics United States	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region

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Results: 21 to 40 of 47

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: 21 to 40 of 47

Results: 21 to 40 of 47