Clinical and research tests for C0919267 - Genetic Testing Registry (GTR) - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

<< First < Prev

Page 2 of 5

Results: 21 to 40 of 93

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Top 99 Genetic Causes of Developmental Delay Panel PreventionGenetics, part of Exact Sciences United States	170	99	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Variant Resolution Test for CancerNext® (+RNAinsight®) Ambry Genetics United States	36	39	D Deletion/duplication analysis R RNA analysis C Sequence analysis of the entire coding region
Invitae Genetic Health Screen Labcorp Genetics (formerly Invitae) LabCorp United States	409	164	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Cancer Screen Labcorp Genetics (formerly Invitae) LabCorp United States	160	62	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Variant Resolution Test for CustomNext-Cancer® (+RNAinsight®) Ambry Genetics United States	90	90	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	88	90	D Deletion/duplication analysis R RNA analysis C Sequence analysis of the entire coding region
CDH1 gene sequence and deletion/duplication Ambry Genetics United States	6	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
CustomNext-Cancer® Ambry Genetics United States	94	90	D Deletion/duplication analysis C Sequence analysis of the entire coding region
CancerNext® Ambry Genetics United States	37	39	D Deletion/duplication analysis C Sequence analysis of the entire coding region
CancerNext-Expanded® Ambry Genetics United States	86	89	D Deletion/duplication analysis C Sequence analysis of the entire coding region
BRCAPlus® Ambry Genetics United States	11	13	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary Breast and Ovarian Cancer - Expanded and Lynch Syndrome Panel PreventionGenetics, part of Exact Sciences United States	29	33	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Hereditary Breast and Ovarian Cancer - High Risk and Lynch Syndrome Panel PreventionGenetics, part of Exact Sciences United States	19	17	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Hereditary Ovarian Cancer Panel PreventionGenetics, part of Exact Sciences United States	40	30	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Invitae Hereditary Hyperekplexia Panel Labcorp Genetics (formerly Invitae) LabCorp United States	23	13	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Epilepsy Panel Labcorp Genetics (formerly Invitae) LabCorp United States	466	297	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Dystonia Comprehensive Panel Labcorp Genetics (formerly Invitae) LabCorp United States	61	38	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Panel for Individualized Cancer Threatment GeneKor MSA Greece	16	52	D Deletion/duplication analysis X Mutation scanning of select exons E Sequence analysis of select exons T Targeted variant analysis
CDH1 MLPA Institute for Human Genetics University Medical Center Freiburg Germany	6	1	D Deletion/duplication analysis
OncoGeneDx Custom Panel GeneDx United States	103	82	D Deletion/duplication analysis C Sequence analysis of the entire coding region

<< First < Prev

Page 2 of 5

Results: 21 to 40 of 93

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.