dbVar for Gene (Select 3587) - 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
nsv7093918	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr11: 116,660,844-117,870,356 , GRCh38.p12 chr11: 116,790,128-117,999,641	PAFAH1B2, FXYD2, 26 more genes
nsv7093833	copy number variation	6	nstd102	human	Uncertain significance	GRCh37 chr11: 116,691,583-121,500,272 , GRCh38.p12 chr11: 116,820,867-121,629,563	RN7SL688P, MIR4492, 131 more genes
nsv7093753	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 117,209,303-120,133,495 , GRCh38.p12 chr11: 117,338,587-120,262,786	TMEM25, HYOU1, 93 more genes
nsv7062420	inversion	1	nstd229	human		GRCh38 chr11: 117,681,463-119,526,734 , GRCh37.p13 chr11: 117,552,178-119,397,444	RN7SL688P, MIR4492, 72 more genes
nsv6580399	inversion	1	nstd223	human		GRCh38 chr11: 117,990,936-117,991,844 , GRCh37.p13 chr11: 117,861,651-117,862,559	IL10RA
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
nsv6309092	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 117,869,800-117,869,856 , GRCh38 chr11: 117,999,085-117,999,141	IL10RA, SMIM35
nsv6308962	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 116,660,844-121,500,272 , GRCh38.p12 chr11: 116,790,128-121,629,563	LOC107984399, PCSK7, 132 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
nsv6290834	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956	CARD17P, RNA5SP350, 480 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
nsv6131836	copy number variation	1	nstd213	human		GRCh37 chr11: 117,740,000-117,930,001 , GRCh38.p12 chr11: 117,869,285-118,059,286	IL10RA, FXYD6, 3 more genes
nsv5564287	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 117,857,030-117,857,362 , GRCh38 chr11: 117,986,315-117,986,647	IL10RA
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
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
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

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Items: 1 to 20 of 112

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Number of Variants: 20

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