dbVar for Gene (Select 3014) - 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
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
nsv7074550	inversion	1	nstd229	human		GRCh38 chr11: 118,332,309-119,477,352 , GRCh37.p13 chr11: 118,203,024-119,348,063	VPS11, LOC100131626, 55 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
nsv6916144	copy number variation	1	nstd229	human		GRCh38 chr11: 119,095,048-119,095,387 , GRCh37.p13 chr11: 118,965,758-118,966,097	H2AX, DPAGT1
nsv6903640	copy number variation	1	nstd229	human		GRCh38 chr11: 118,856,131-119,169,941 , GRCh37.p13 chr11: 118,726,840-119,040,650	CENATAC, DPAGT1, 19 more genes
nsv6902025	copy number variation	1	nstd229	human		GRCh38 chr11: 118,757,701-119,235,300 , GRCh37.p13 chr11: 118,635,052-119,106,010	UPK2, VPS11, 25 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
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
nsv6291385	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 118,849,155-119,067,781 , GRCh38.p12 chr11: 118,978,445-119,197,071	RPS25, C2CD2L, 17 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
nsv6143009	copy number variation	1	nstd206	human		GRCh38 chr11: 119,058,364-119,114,364 , GRCh37.p13 chr11\|NW_003871076.1: 79,964-108,875 , GRCh37.p13 chr11: 118,929,075-118,957,986	, DPAGT1, 4 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
nsv4682817	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 118,895,600-118,972,385 , GRCh38.p12 chr11\|NW_009646203.1: 46,490-108,875 , GRCh38.p12 chr11: 119,024,890-119,101,675	VPS11, HMBS, 4 more genes
nsv4682533	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 118,962,110-118,964,270 , GRCh38.p12 chr11: 119,091,400-119,093,560	H2AX, HMBS
nsv4681127	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 118,958,944-118,964,270 , GRCh38.p12 chr11: 119,088,234-119,093,560	HMBS, H2AX
nsv4675236	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 118,280,670-119,650,105 , GRCh38.p12 chr11: 118,409,955-119,779,396	SETP16, UPK2, 59 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

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Has Clinical Interpretation

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Items: 1 to 20 of 121

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Number of Variants: 20

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