Clinical and research tests for SMARCA4 - Genetic Testing Registry (GTR)

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Hereditary Breast and Ovarian Cancer Panel QDx Pathology Services, Inc. United States	3	23	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Clariti 20/20 QDx Pathology Services, Inc. United States	15	44	D Deletion/duplication analysis C Sequence analysis of the entire coding region
NeXT Dx Personalis, Inc. United States	1	413	I Microsatellite instability testing (MSI) R RNA analysis C Sequence analysis of the entire coding region
Coffin-Siris syndrome Panel Genetic Services Laboratory University of Chicago United States	7	15	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Tempus xT Tempus AI - RTP United States	2	647	I Microsatellite instability testing (MSI) C Sequence analysis of the entire coding region
OnkoRisk Hereditary Oncology Plus Panel BioReference Health United States	97	77	C Sequence analysis of the entire coding region
SMARCA4 Gene Mental retardation, autosomal dominant type 16 NGS Genetic DNA Test DNA Labs India India	1	1	S Mutation scanning of the entire coding region
Hereditary Renal Cancer Panel Mayo Clinic Laboratories Mayo Clinic United States	1	19	C Sequence analysis of the entire coding region
Hereditary Expanded Cancer Panel Mayo Clinic Laboratories Mayo Clinic United States	1	86	C Sequence analysis of the entire coding region
Tempus xT Tempus AI - CHI United States	2	647	I Microsatellite instability testing (MSI) C Sequence analysis of the entire coding region
Rhabdoid Tumor Predisposition Syndrome NGS Panel UAB Medical Genomics Laboratory UAB Medicine United States	5	2	D Deletion/duplication analysis C Sequence analysis of the entire coding region
FoundationOne® Heme Foundation Medicine, Inc. United States	2	405	D Deletion/duplication analysis R RNA analysis E Sequence analysis of select exons C Sequence analysis of the entire coding region
Small cell carcinoma of the ovary, hypercalcemic type Molecular Genetics Laboratory North York General Hospital Canada	1	1	C Sequence analysis of the entire coding region
Rhabdoid predisposition syndrome Molecular Genetics Laboratory North York General Hospital Canada	1	2	C Sequence analysis of the entire coding region
Comprehensive cancer panel (76 genes) Molecular Genetics Laboratory North York General Hospital Canada	1	74	T Targeted variant analysis
NEXT GEN SEQUENCING COMPREHENSIVE SOLID TUMOR PANEL Alverno Laboratories United States	1	27	T Targeted variant analysis
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
OnkoSight Advanced Bladder Cancer Panel BioReference Health United States	1	39	C Sequence analysis of the entire coding region
Common Hereditary Cancer Screening Panel PreventionGenetics, part of Exact Sciences United States	94	55	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
CentoBreast Centogene AG - the Rare Disease Company Germany	58	28	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.

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Results: 1 to 20 of 180

Results: 1 to 20 of 180