Clinical and research tests for C2931038 - 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
Hereditary Pancreatic Cancer Panel Mayo Clinic Laboratories Mayo Clinic United States	1	12	C Sequence analysis of the entire coding region
Otogenetics Hereditary Cancers Otogenetics United States	36	39	E Sequence analysis of select exons
Hereditary Pancreatic Cancer (BRCA2, PALB2) GeneKor MSA Greece	2	2	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary Melanoma and/or Pancreatic Cancer, CDKN2A Gene GeneKor MSA Greece	3	1	C Sequence analysis of the entire coding region
Hereditary GI cancer panel (31 genes) Molecular Genetics Laboratory North York General Hospital Canada	13	31	C Sequence analysis of the entire coding region
myRisk Hereditary Cancer Myriad Genetics, Inc. United States	32	46	D Deletion/duplication analysis C Sequence analysis of the entire coding region
ColoGene GeneID Lab - Advanced Molecular Diagnostics United States	41	19	C Sequence analysis of the entire coding region
myRisk Single Site Analysis Myriad Genetics, Inc. United States	32	45	T Targeted variant analysis
Hereditary pancreatic cancer panel CHEO Genetics Diagnostic Laboratory Children's Hospital of Eastern Ontario Canada	1	12	C Sequence analysis of the entire coding region
Hereditary Pancreatic Cancer Core Panel Blueprint Genetics Finland	1	5	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Pancreatic Cancer: Gene Deletion/Duplication Panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	1	14	D Deletion/duplication analysis
Pancreatic Cancer: Gene Sequencing Panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	1	14	C Sequence analysis of the entire coding region
Invitae Pediatric Solid Tumors Panel Labcorp Genetics (formerly Invitae) LabCorp United States	90	48	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Multi-Cancer Panel Labcorp Genetics (formerly Invitae) LabCorp United States	138	80	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Inherited Cancer Panel Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University United States	33	49	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Common Hereditary Cancers Panel (Breast, Gyn, GI) Labcorp Genetics (formerly Invitae) LabCorp United States	75	42	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Pancreatic cancer Panel CeGaT GmbH Germany	6	17	C Sequence analysis of the entire coding region
Pancreatic Cancer MGZ Medical Genetics Center Germany	1	11	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.