Clinical and research tests for C1708353 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
myRisk Hereditary Cancer Myriad Genetics, Inc. United States	32	46	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary Pheochromocytoma and Paraganglioma Panel Genetic Services Laboratory University of Chicago United States	10	16	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary Paraganglioma-Pheochromocytoma Expanded Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	12	12	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary Paraganglioma-Pheochromocytoma (SDHA, SDHB, SDHC, and SDHD) Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	1	4	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary Endocrine Cancer Panel (12 Genes) Quest Diagnostics Nichols Institute San Juan Capistrano United States	6	12	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Hereditary Cancer Panel (66 Genes) Quest Diagnostics Nichols Institute San Juan Capistrano United States	35	66	D Deletion/duplication analysis 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
Endocrine tumours Institute of Human Genetics Cologne University Germany	17	11	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary Thyroid Cancer Panel Genetic Services Laboratory University of Chicago United States	11	13	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary Paraganglioma-Pheochromocytoma Panel Blueprint Genetics Finland	1	11	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary Pediatric Cancer Panel Blueprint Genetics Finland	6	71	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Metabolic Epilepsy Panel Blueprint Genetics Finland	8	41	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
PGL/PCC (Paraganglioma/Pheochromocytoma) Panel GeneDx United States	2	12	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Sarcoma Panel Invitae United States	27	26	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Renal/Urinary Tract Cancers Panel Invitae United States	37	24	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Multi-Cancer Panel Invitae United States	139	80	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Hereditary Paraganglioma-Pheochromocytoma Panel Invitae United States	10	10	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Gastric Cancer Panel Invitae United States	28	18	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Common Hereditary Cancers Panel (Breast, Gyn, GI) Invitae United States	75	42	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.