dbVar for Gene (Select 915) - 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
nsv5507162	copy number variation	1	nstd206	human		GRCh38 chr11: 118,338,781-118,338,869 , GRCh37.p13 chr11: 118,209,496-118,209,584	CD3D
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	FAUP4, MMP7, 2031 more genes
nsv4838360	copy number variation	1	nstd200	human		GRCh37 chr11: 118,209,496-118,209,584 , GRCh38.p12 chr11: 118,338,781-118,338,869	CD3D
nsv4732750	copy number variation	1	nstd199	human		GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572	, LINC02702, 392 more genes
nsv4683551	copy number variation	9	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr11: 117,856,768-118,972,385 , GRCh38.p12 chr11: 117,986,053-119,101,675	MIR6716, TREHP1, 48 more genes
nsv4674572	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571	ACRV1, APLP2, 382 more genes
nsv4455281	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 117,830,263-134,938,470 , GRCh38.p12 chr11: 117,959,548-135,068,576	NTM-AS1, LOC403312, 369 more genes
nsv4451218	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 118,007,722-119,170,511 , GRCh38.p12 chr11: 118,137,007-119,299,801	ABCG4, CCDC153, 52 more genes
nsv4349506	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 116,691,675-134,889,485 , GRCh38.p12 chr11: 116,820,959-135,019,591	LOC107984407, DCPS, 394 more genes
nsv4349045	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 116,700,253-134,904,063 , GRCh38.p12 chr11: 116,829,537-135,034,169	MPZL3, ADAMTS8, 393 more genes
nsv3923375	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 116,722,088-134,868,420 , NCBI36 chr11: 116,227,298-134,373,630 , GRCh38 chr11: 116,851,372-134,998,526	VPS26B, LOC105369531, 390 more genes
nsv3922253	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 100,219,331-134,910,140 , NCBI36 chr11: 99,724,541-134,415,350 , GRCh38 chr11: 100,348,599-135,040,246	RPS27P19, UBASH3B, 655 more genes
nsv3916857	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr11: 116,227,321-134,373,617 , GRCh37 chr11: 116,722,111-134,868,407 , GRCh38 chr11: 116,851,395-134,998,513	RPUSD4, ELOCP22, 390 more genes
nsv3913230	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 113,444,446-120,648,921 , NCBI36 chr11: 112,820,378-120,024,840 , GRCh37 chr11: 113,315,168-120,519,630	ARHGEF12, LOC105369526, 169 more genes
nsv3912905	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 112,864,326-131,189,315 , GRCh37 chr11: 112,832,130-131,059,210 , NCBI36 chr11: 112,240,259-130,564,420	SLC37A2, OR6X1, 416 more genes
nsv3911830	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 116,182,194-134,450,377 , GRCh37 chr11: 116,676,984-134,945,165 , GRCh38 chr11: 116,806,268-135,075,271	ACRV1, BMPR1AP2, 395 more genes
nsv3911822	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 116,709,878-127,084,261 , GRCh37 chr11: 117,204,668-127,579,051 , GRCh38 chr11: 117,333,952-127,709,156	LOC105369540, C1QTNF5, 283 more genes
nsv3911440	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 116,244,861-134,450,377 , GRCh37 chr11: 116,739,651-134,945,165 , GRCh38 chr11: 116,868,935-135,075,271	RN7SL688P, ARHGEF12, 391 more genes
nsv3909122	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 115,215,434-120,559,928 , GRCh38.p12 chr11: 115,344,715-120,689,219	LOC107984393, CENATAC-DT, 136 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	IGHMBP2, SYTL2, 2829 more genes

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Organism

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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 101

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Number of Variants: 20

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