dbVar for Gene (Select 103344931) - 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
nsv4456626	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 114,544,537-135,427,143 , GRCh38.p12 chr10: 112,784,778-133,613,639	LOC105378521, ZRANB1, 317 more genes
nsv4348764	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 110,022,170-135,439,095 , GRCh38.p12 chr10: 108,262,412-133,625,591	LOC105378492, VENTX, 373 more genes
nsv4339713	sequence alteration	1	nstd166	human		GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970	, ADRA2A, 1651 more genes
nsv3923859	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 113,062,847-135,284,168 , GRCh37 chr10: 113,072,857-135,434,178 , GRCh38 chr10: 111,313,099-133,620,674	AS-PTPRE, SFXN4, 330 more genes
nsv3923769	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 100,194,215-132,432,797 , GRCh37 chr10: 101,953,972-134,246,301 , NCBI36 chr10: 101,943,962-134,096,291	LOC105378493, LINC02627, 477 more genes
nsv3922500	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr10: 112,554,483-116,633,759 , GRCh37 chr10: 112,564,493-116,643,769 , GRCh38 chr10: 110,804,735-114,884,010	ADRA2A, ADRB1, 57 more genes
nsv3922274	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr10: 103,274,160-135,374,737 , GRCh37.p13 chr10: 103,284,170-135,524,747 , GRCh38.p12 chr10: 101,524,413-133,787,422	DPCD, LOC105378467, 504 more genes
nsv3921919	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 100,600,492-133,622,588 , GRCh37 chr10: 102,360,249-135,436,092 , NCBI36 chr10: 102,350,239-135,286,082	MIR4295, BORCS7, 508 more genes
nsv3920295	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422	EIF2S2P3, CYP17A1-AS1, 895 more genes
nsv3919820	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 107,191,100-118,761,489 , GRCh37 chr10: 108,950,858-120,521,001 , NCBI36 chr10: 108,940,848-120,510,991	CCDC186, RN7SKP288, 147 more genes
nsv3916477	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 104,481,920-115,834,854 , GRCh37 chr10: 104,491,930-115,844,864 , GRCh38 chr10: 102,732,173-114,085,105	XPNPEP1, NRAP, 147 more genes
nsv3915987	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 112,074,094-115,537,174 , GRCh37 chr10: 113,833,852-117,032,437 , NCBI36 chr10: 113,823,842-117,286,674	LOC103344931, LINC02626, 48 more genes
nsv3914619	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 111,418,518-126,431,209 , GRCh37.p13 chr10: 111,428,528-126,441,219 , GRCh38.p12 chr10: 109,668,770-124,752,650	LOC103344931, LINC02626, 225 more genes
nsv3912079	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 109,852,335-135,284,168 , GRCh38 chr10: 108,102,587-133,620,674 , GRCh37 chr10: 109,862,345-135,434,178	TUBGCP2, SHOC2, 372 more genes
nsv3911051	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr10: 114,450,935-122,720,120 , GRCh37 chr10: 114,460,945-122,730,130 , GRCh38 chr10: 112,701,186-120,970,617	ADRB1, CASP7, 123 more genes
nsv3909942	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 96,872,364-118,383,651 , GRCh38 chr10: 95,112,607-116,776,637 , NCBI36 chr10: 96,862,354-118,526,138	LOC102723665, SFR1, 360 more genes
nsv3908254	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 106,003,533-135,427,143 , GRCh38.p12 chr10: 104,243,775-133,613,639	MIR4680, BCCIP, 404 more genes
nsv3907664	copy number variation	1	nstd102	human	drug response	GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422	SHOC2, FAM245B, 1487 more genes
nsv3906389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996	LOC100419870, LOC102724439, 2105 more genes
nsv3905499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 104,030,479-115,410,590 , GRCh38.p12 chr10: 102,270,722-113,650,831	RPS15AP30, PDCD11, 156 more genes

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Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 102

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Number of Variants: 20

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