Clinical and research tests for C0476089 - Genetic Testing Registry (GTR)

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Results: 41 to 60 of 193

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
KRAS, BRAF, and NRA Mutation Analysis PathGroup United States	23	3	T Targeted variant analysis
KRAS, BRAF, NRAS and MSI Mutation Analysis PathGroup United States	23	3	T Targeted variant analysis
BRAF, EGFR, KRAS Mutation Analysis PathGroup United States	25	3	T Targeted variant analysis
Endometrial and/or Uterine Cancer Panel IntelligeneCG LLC United States	5	7	C Sequence analysis of the entire coding region
Variant Resolution Test for CancerNext® (+RNAinsight®) Ambry Genetics United States	79	18	D Deletion/duplication analysis R RNA analysis C Sequence analysis of the entire coding region
Invitae Genetic Health Screen Invitae United States	409	164	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Cancer Screen Invitae United States	160	62	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae 78 Gene Actionable Disorders Panel Invitae United States	220	75	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Variant Resolution Test for CustomNext-Cancer® (+RNAinsight®) Ambry Genetics United States	147	18	D Deletion/duplication analysis R RNA analysis C Sequence analysis of the entire coding region
Variant Resolution Test for MelanomaNext® (+RNAinsight®) Ambry Genetics United States	40	3	D Deletion/duplication analysis R RNA analysis C Sequence analysis of the entire coding region
Variant Resolution Test for BrainTumorNext® (+RNAinsight®) Ambry Genetics United States	72	8	D Deletion/duplication analysis R RNA analysis C Sequence analysis of the entire coding region
Variant Resolution Test for ProstateNext® (+RNAinsight®) Ambry Genetics United States	40	11	D Deletion/duplication analysis R RNA analysis C Sequence analysis of the entire coding region
Variant Resolution Test for ColoNext® (+RNAinsight®) Ambry Genetics United States	48	10	D Deletion/duplication analysis R RNA analysis C Sequence analysis of the entire coding region
Variant Resolution Test for PancNext® plus Pancreatitis (+RNAinsight®) Ambry Genetics United States	41	10	D Deletion/duplication analysis R RNA analysis C Sequence analysis of the entire coding region
Variant Resolution Test for PancNext® (+RNAinsight®) Ambry Genetics United States	41	10	D Deletion/duplication analysis R RNA analysis C Sequence analysis of the entire coding region
Variant Resolution Test for RenalNext® (+RNAinsight®) Ambry Genetics United States	57	7	D Deletion/duplication analysis R RNA analysis C Sequence analysis of the entire coding region
Variant Resolution Test for CancerNext-Expanded® (+RNAinsight®) Ambry Genetics United States	141	18	D Deletion/duplication analysis R RNA analysis C Sequence analysis of the entire coding region
PancNext® plus Pancreatitis Ambry Genetics United States	41	19	D Deletion/duplication analysis C Sequence analysis of the entire coding region
PrimBio Cancer HotSpot Panel PrimBio Research Institute United States	60	50	T Targeted variant analysis
RenalNext® Ambry Genetics United States	57	20	D Deletion/duplication analysis C Sequence analysis of the entire coding region

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Results: 41 to 60 of 193

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: 41 to 60 of 193

Results: 41 to 60 of 193