Clinical and research tests for C5399763 AND 500105 - Genetic Testing Registry (GTR) - NCBI

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Results: 1 to 13 of 13

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
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
EPM2AIP1 Single Gene Fulgent Genetics United States	3	1	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
Pancreatic Cancer Comprehensive Panel Fulgent Genetics United States	55	22	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Nervous System / Brain Cancer Comprehensive Panel Fulgent Genetics United States	133	27	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Thyroid Cancer Comprehensive Panel Fulgent Genetics United States	37	7	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Colorectal Cancer Focus Panel Fulgent Genetics United States	62	18	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Clinical Exome Fulgent Genetics United States	5128	4672	D Deletion/duplication analysis C Sequence analysis of the entire coding region
APC Single Gene Fulgent Genetics United States	4	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region

Results: 1 to 13 of 13

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.