Clinical and research tests for C1861906 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Expedio Hereditary Cancer Predisposition Screening Assay Kailos Genetics United States	40	31	C Sequence analysis of the entire coding region
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 C Sequence analysis of the entire coding region
OnkoRisk Hereditary Oncology Plus Panel BioReference Health United States	97	77	C Sequence analysis of the entire coding region
OnkoRisk Hereditary Oncology Management Panel BioReference Health United States	47	17	C Sequence analysis of the entire coding region
OnkoRisk Hereditary Oncology Guideline Panel BioReference Health United States	71	54	C Sequence analysis of the entire coding region
OnkoRisk Women's Hereditary Cancer Panel BioReference Health United States	34	18	C Sequence analysis of the entire coding region
Otogenetics Hereditary Cancers Otogenetics United States	36	39	E Sequence analysis of select exons
BRCA2 Gene Sequencing Michigan Medical Genetics Laboratories University of Michigan United States	7	1	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 gene sequencing Michigan Medical Genetics Laboratories University of Michigan United States	7	1	C Sequence analysis of the entire coding region
BRCA1 deletion/duplication testing Michigan Medical Genetics Laboratories University of Michigan United States	7	1	D Deletion/duplication analysis
BRCA1 and BRCA2 Sequencing and Del/Dup Michigan Medical Genetics Laboratories University of Michigan United States	8	2	C Sequence analysis of the entire coding region
Li Fraumeni Syndrome Molecular Genetics Laboratory London Health Sciences Centre Canada	5	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Tier 1 Hereditary Conditions Test Color Diagnostics, LLC DBA Color Health United States	14	10	C Sequence analysis of the entire coding region
Endeavor PathGroup United States	73	505	C Sequence analysis of the entire coding region
Hereditary Cancer Test Color Diagnostics, LLC DBA Color Health United States	24	29	C Sequence analysis of the entire coding region
Hereditary breast/ovarian cancer - analysis the BRCA1 gene mutations in accordance with EMQN recommendations Laboratory of Human Genetics GENOMED Health Care Center Poland	6	1	C Sequence analysis of the entire coding region
Hereditary breast/ovarian cancer - analysis the BRCA2 gene mutations in accordance with EMQN recommendations Laboratory of Human Genetics GENOMED Health Care Center Poland	6	1	C Sequence analysis of the entire coding region
Hereditary Disease Risk Test Color Diagnostics, LLC DBA Color Health United States	51	59	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.