dbVar for Gene (Select 80218) - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5453590	copy number variation	1	nstd206	human		GRCh38 chr3: 113,723,542-113,723,958 , GRCh37.p13 chr3: 113,442,389-113,442,805	NAA50
nsv5445908	copy number variation	1	nstd206	human		GRCh38 chr3: 113,721,937-113,722,854 , GRCh37.p13 chr3: 113,440,784-113,441,701	NAA50
nsv5444632	copy number variation	1	nstd206	human		GRCh38 chr3: 113,722,921-113,723,420 , GRCh37.p13 chr3: 113,441,768-113,442,267	NAA50
nsv5374641	translocation	1	nstd200	human		GRCh38 chr3: 113,742,027-113,742,027 , GRCh38 chr1: 21,390,147-21,390,147 , GRCh37.p13 chr1: 21,716,640-21,716,640 , GRCh37.p13 chr3: 113,460,874-113,460,874	NAA50
nsv5199610	mobile element insertion	1	nstd203	human		GRCh38 chr3: 113,742,009-113,742,028 , GRCh37.p13 chr3: 113,460,856-113,460,875	NAA50
nsv5036857	inversion	1	nstd200	human		GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646	, FBRSL1P1, 801 more genes
nsv5031637	inversion	1	nstd200	human		GRCh38 chr3: 112,181,184-125,673,487 , GRCh37.p13 chr3: 111,900,031-125,392,331	, ARHGAP31, 218 more genes
nsv4728380	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 112,135,341-115,509,260 , GRCh38.p12 chr3: 112,416,494-115,790,413	SLC35A5, EIF4E2P2, 51 more genes
nsv4709093	copy number variation	1	nstd195	human		GRCh37 chr3: 113,440,783-113,440,784 , GRCh38.p12 chr3: 113,721,936-113,721,937	NAA50
nsv4684086	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 113,233,952-118,525,556 , GRCh38.p12 chr3: 113,515,105-118,806,709	SIDT1, RNU5E-8P, 55 more genes
nsv4584665	copy number variation	1	nstd183	human		GRCh37 chr3: 112,890,620-113,680,951 , GRCh38.p12 chr3: 113,171,773-113,962,104	NEPRO-AS1, SIDT1, 17 more genes
nsv4578248	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 112,183,943-115,492,949 , GRCh38.p12 chr3: 112,465,096-115,774,102	ZBTB20, ZBTB20-AS1, 51 more genes
nsv4317801	inversion	1	nstd166	human		GRCh37.p13 chr3: 106,160,269-123,476,086 , GRCh38.p12 chr3: 106,441,422-123,757,239	, ADPRH, 270 more genes
nsv4091559	copy number variation	1	nstd166	human		GRCh37.p13 chr3: 113,440,784-113,441,751 , GRCh38.p12 chr3: 113,721,937-113,722,904	NAA50
nsv4084755	copy number variation	1	nstd166	human		GRCh37.p13 chr3: 113,442,389-113,442,805 , GRCh38.p12 chr3: 113,723,542-113,723,958	NAA50
nsv4074546	copy number variation	1	nstd166	human		GRCh37.p13 chr3: 113,448,588-113,603,588 , GRCh38.p12 chr3: 113,729,741-113,884,741	NAA50, GRAMD1C, 3 more genes
nsv3924149	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 113,666,631-116,975,648 , GRCh38 chr3: 112,465,094-115,774,111 , GRCh37 chr3: 112,183,941-115,492,958	ATOSBP1, ZBTB20-AS1, 51 more genes
nsv3922717	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168	OR7E53P, HSPA8P9, 794 more genes
nsv3922321	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 113,681,019-116,975,639 , GRCh38 chr3: 112,479,482-115,774,102 , GRCh37 chr3: 112,198,329-115,492,949	NAA50, ATOSBP1, 51 more genes
nsv3918981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446	LINC02614, LINC02054, 1469 more genes

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Number of Variants: 20

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dbVar

Result Filters

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Organism

Variant Type

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Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 186

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Number of Variants: 20

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