Clinical and research tests for C1333600 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
OncoAlly™ Hereditary Colorectal Cancer Analysis Variantyx, Inc. United States	1	21	D Deletion/duplication analysis X Mutation scanning of select exons C Sequence analysis of the entire coding region
OncoAlly™ Common Hereditary Cancers Analysis Variantyx, Inc. United States	1	46	D Deletion/duplication analysis X Mutation scanning of select exons C Sequence analysis of the entire coding region
OncoAlly™ Comprehensive Hereditary Cancer Analysis Variantyx, Inc. United States	1	88	D Deletion/duplication analysis X Mutation scanning of select exons C Sequence analysis of the entire coding region
OncoAlly™ BRCA1/2 Analysis Analysis Variantyx, Inc. United States	2	2	D Deletion/duplication analysis C Sequence analysis of the entire coding region
CancerNext® Ambry Genetics United States	80	34	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary Cancer Panel Mendelics Brazil	1	37	C Sequence analysis of the entire coding region
Hereditary Cancer Panel (Complete) Mendelics Brazil	1	264	C Sequence analysis of the entire coding region
OncoAlly™ Cancer Predisposition Variantyx, Inc. United States	2	87	D Deletion/duplication analysis X Mutation scanning of select exons C Sequence analysis of the entire coding region
Hereditary Cancer Testing - Full Panel (76) AIP, APC, ATM, AXIN2, BAP1, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDC73, CDH1, CDK4, CDKN1B, CDKN2A, CHEK2, CTNN1, DICER1, EGFR, EGLN1, EPCAM, EXT1, EXT2, FH, FLCN, GALNT12, GREM1, HOXB13, KIT, LZTR1, MAX, MEN1, M Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System Canada	1	78	S Mutation scanning of the entire coding region
AXIN2-related Attenuated Familial Adenomatous Polyposis Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System Canada	1	1	S Mutation scanning of the entire coding region
BAP1 Tumour Predisposition Syndrome Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System Canada	1	1	S Mutation scanning of the entire coding region
Birt-Hogg-Dube Syndrome Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System Canada	1	1	S Mutation scanning of the entire coding region
Carney Complex Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System Canada	1	1	S Mutation scanning of the entire coding region
CHRPE, CMV Thyroid, Desmoid Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System Canada	1	1	S Mutation scanning of the entire coding region
CHRPE, CMV Thyroid, Desmoid with MUTYH Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System Canada	1	2	S Mutation scanning of the entire coding region
DICER-associated Syndrome Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System Canada	1	1	S Mutation scanning of the entire coding region
Dysplastic Nevus Syndrome Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System Canada	1	2	S Mutation scanning of the entire coding region
Familial Isolated Pituitary Adenoma Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System Canada	1	1	S Mutation scanning of the entire coding region
Hereditary Hyperparathyroidism Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System Canada	1	2	S Mutation scanning of the entire coding region
Hereditary Leiomyomatosis and Renal Cell Cancer Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System Canada	1	1	S Mutation scanning 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.