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

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Results: 21 to 40 of 44

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
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
Hereditary Cancer Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	33	73	D Deletion/duplication analysis E Sequence analysis of select exons C Sequence analysis of the entire coding region
Pheochromocytoma and Paraganglioma Panel CeGaT GmbH Germany	7	13	C Sequence analysis of the entire coding region
Hereditary Paraganglioma-Pheochromocytoma Syndromes, SDHB sequencing Molecular Diagnostics Laboratory Seoul National University Hospital South Korea	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Cancer Predisposition Asper Biogene Asper Biogene LLC Estonia	135	98	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary Renal Cancer Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	14	21	D Deletion/duplication analysis X Mutation scanning of select exons C Sequence analysis of the entire coding region
Hereditary Gastrointestinal Cancer Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	22	26	D Deletion/duplication analysis E Sequence analysis of select exons C Sequence analysis of the entire coding region
PCC Syndrome Institute of Human Genetics Cologne University Germany	1	1	C Sequence analysis of the entire coding region
Hereditary Phaeochromocytoma/Paraganglioma Syndromes (MAX, SDHAF2, SDHB, SDHC, SDHD, TMEM127, VHL) Molecular Genetics Laboratory - Diagnostics Genetics LabPLUS - Auckland City Hospital New Zealand	6	7	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Paraganglioma, SDHB GGA - Galil Genetic Analysis Israel	1	1	C Sequence analysis of the entire coding region

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Results: 21 to 40 of 44

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.