dbVar for Gene (Select 406882) - 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
nsv7137129	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659	VSIG10L2, OR8B6P, 268 more genes
nsv7059023	inversion	1	nstd229	human		GRCh38 chr11: 121,250,599-123,864,348 , GRCh37.p13 chr11: 121,121,308-123,735,056	MIR4493, SF3A3P2, 49 more genes
nsv6899398	copy number variation	1	nstd229	human		GRCh38 chr11: 122,134,701-122,166,000 , GRCh37.p13 chr11: 122,005,409-122,036,708	MIRLET7A2, MIR100HG, 2 more genes
nsv6591553	inversion	1	nstd223	human		GRCh38 chr11: 119,568,183-123,189,997 , GRCh37.p13 chr11: 119,438,894-123,060,705	UBASH3B, LOC105369529, 66 more genes
nsv6584901	inversion	1	nstd223	human		GRCh38 chr11: 120,551,312-124,267,280 , GRCh37.p13 chr11: 120,422,021-124,137,176	RNU6-256P, CLMP, 85 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	PYGM, ATL3, 2125 more genes
nsv6291074	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847	ZW10, MPZL2, 378 more genes
nsv6289927	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522	IGSF9B, MIR10526, 592 more genes
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
nsv4675832	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 120,742,540-134,938,470 , GRCh38.p12 chr11: 120,871,831-135,068,576	MIR8052, BLID, 275 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
nsv4436748	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 120,576,984-134,934,063 , GRCh38.p12 chr11: 120,706,275-135,064,169	LINC02098, LOC105369587, 276 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
nsv3924566	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 120,507,265-134,576,266 , NCBI36 chr11: 119,883,184-133,951,370 , GRCh37 chr11: 120,377,974-134,446,160	CCDC15-DT, LOC105369544, 271 more genes
nsv3923916	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 120,296,802-124,641,109 , NCBI36 chr11: 119,802,012-124,146,319 , GRCh38 chr11: 120,426,093-124,771,213	OR8B2, OR8G5, 120 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
nsv3923251	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 119,891,678-134,450,377 , GRCh38 chr11: 120,515,759-135,075,271 , GRCh37 chr11: 120,386,468-134,945,165	KIRREL3-AS3, OR8B4, 279 more genes
nsv3922773	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 119,304,619-134,868,407 , GRCh38 chr11: 119,433,909-134,998,513 , NCBI36 chr11: 118,809,829-134,373,617	ETS1-AS1, SLC37A2, 301 more genes

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Number of Variants: 20

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Items: 1 to 20 of 123

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Number of Variants: 20

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