Clinical and research tests for C2674616 - 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
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
Hereditary Colon and Endometrial Cancer-ColoNGS GeneKor MSA Greece	10	7	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Familial Adenomatosis Polyposis GeneKor MSA Greece	5	2	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Inherited Cancer Panel Dhiti Omics Technologies Private Ltd India	136	84	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
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
Sarcoma Comprehensive Panel Fulgent Genetics United States	70	26	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Colorectal Cancer Comprehensive Panel Fulgent Genetics United States	77	22	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Gastric Cancer Comprehensive Panel Fulgent Genetics United States	37	15	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

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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.