Clinical and research tests for C4016951 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Hereditary Cancer Panel Comprehensive Molecular Genetics Laboratory London Health Sciences Centre Canada	39	30	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
BRCA2-Hereditary Cancer of the Breast Molecular Genetics Laboratory London Health Sciences Centre Canada	5	1	D Deletion/duplication analysis E Sequence analysis of select exons C Sequence analysis of the entire coding region
Hereditary Cancer Panel - High Penetrance 16 Molecular Genetics Laboratory London Health Sciences Centre Canada	28	16	D Deletion/duplication analysis E Sequence analysis of select exons C Sequence analysis of the entire coding region
BRCA2 deletion/duplication testing Michigan Medical Genetics Laboratories University of Michigan United States	6	1	D Deletion/duplication analysis
BRCA1 deletion/duplication testing Michigan Medical Genetics Laboratories University of Michigan United States	7	1	D Deletion/duplication analysis
Li Fraumeni Syndrome Molecular Genetics Laboratory London Health Sciences Centre Canada	5	1	D Deletion/duplication analysis E Sequence analysis of select exons C Sequence analysis of the entire coding region
VistaSeq Breast Cancer Panel Molecular Diagnostic Laboratory LabCorp United States	16	19	D Deletion/duplication analysis C Sequence analysis of the entire coding region
VisaSeq Breast and GYN Cancer Panel Molecular Diagnostic Laboratory LabCorp United States	32	25	D Deletion/duplication analysis C Sequence analysis of the entire coding region
TP53 sequencing and deletion/duplication Children's Hospital of Los Angeles, Center for Personalized Medicine United States	6	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
OncoGeneDx Custom Panel GeneDx United States	103	82	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Common Cancer Management Panel GeneDx United States	56	37	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Breast Cancer Management Panel GeneDx United States	24	9	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Breast/Gyn Cancer Panel GeneDx United States	46	24	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Common Cancer Panel GeneDx United States	60	47	D Deletion/duplication analysis C Sequence analysis of the entire coding region
ACMG Secondary Findings (Medically Actionable Genes, Including Cardio and Cancer) NGS Panel Fulgent Genetics United States	177	59	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Breast and Ovarian Cancer Focus Panel Fulgent Genetics United States	50	21	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Breast Cancer STAT Fulgent Genetics United States	34	9	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Breast and Ovarian Cancer Comprehensive Panel Fulgent Genetics United States	58	24	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Full Focus Cancer Panel Fulgent Genetics United States	82	30	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Pediatric Solid Tumors Panel Invitae United States	90	48	D Deletion/duplication analysis C Sequence analysis of the entire coding region

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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.