dbVar for Gene (Select 3846) - 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
nsv5919132	copy number variation	1	nstd209	human		GRCh38 chr11: 71,548,924-71,549,067 , GRCh37.p13 chr11: 71,259,970-71,260,113	KRTAP5-9
nsv5597919	copy number variation	1	nstd207	human		GRCh38 chr11: 71,548,924-71,549,067 , GRCh37.p13 chr11: 71,259,970-71,260,113	KRTAP5-9
nsv5495772	copy number variation	1	nstd206	human		GRCh38 chr11: 71,525,696-71,565,696 , GRCh37.p13 chr11: 71,236,742-71,276,742	KRTAP5-9, KRTAP5-8, 2 more genes
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
nsv4751865	inversion	1	nstd199	human		GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187	, ACP2, 1686 more genes
nsv4681893	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 71,146,401-71,907,241 , GRCh38.p12 chr11: 71,435,355-72,196,197	OR7E128P, ZNF705EP, 39 more genes
nsv4208346	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 71,257,060-71,271,657 , GRCh38.p12 chr11: 71,546,014-71,560,611	KRTAP5-9
nsv4205093	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 71,237,543-71,275,844 , GRCh38.p12 chr11: 71,526,497-71,564,798	KRTAP5-10, KRTAP5-7, 2 more genes
nsv3957105	copy number variation	1	nstd168	human		GRCh38 chr11: 71,537,495-71,561,385 , GRCh37.p13 chr11: 71,248,541-71,272,431	KRTAP5-9, KRTAP5-8
nsv3921153	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr11: 71,164,008-72,309,374 , GRCh37 chr11: 71,088,949-72,020,418 , NCBI36 chr11: 70,552,702-71,698,066	LOC220077, PHOX2A, 47 more genes
nsv3919985	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 70,668,528-72,528,680 , GRCh37.p13 chr11: 70,990,880-72,851,032 , GRCh38.p12 chr11: 71,279,834-73,139,987	OR7E128P, OR7E87P, 68 more genes
nsv3917463	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr11: 67,555,736-70,982,189 , GRCh37 chr11: 67,799,160-71,304,541 , GRCh38 chr11: 68,031,693-71,593,495	CCND1, CHKA, 71 more genes
nsv3915827	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 70,530,702-70,972,913 , GRCh37.p13 chr11\|NW_004070871.1: 636,221-872,115 , GRCh37.p13 chr11: 70,853,054-71,295,265 , GRCh38.p12 chr11: 71,142,008-71,584,219	ACTE1P, KRTAP5-14P, 11 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
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	RTN3, KRTAP5-13P, 2833 more genes
nsv3896056	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 71,118,826-71,279,571 , GRCh38.p12 chr11: 71,407,780-71,568,525	ACTE1P, NADSYN1, 8 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	LOC105376598, OSBPL9P2, 2842 more genes
nsv3879694	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr11: 70,520,567-70,966,737 , GRCh37.p13 chr11\|NW_004070871.1: 626,086-872,115 , GRCh37.p13 chr11: 70,842,919-71,289,089 , GRCh38.p12 chr11: 71,131,873-71,578,043	KRTAP5-8, NADSYN1, 10 more genes
nsv3156908	copy number variation	1	nstd151	human		GRCh37 chr11: 71,155,898-71,277,247 , GRCh38.p12 chr11: 71,444,852-71,566,201	KRTAP5-9, MIR6754, 6 more genes
nsv3156561	copy number variation	1	nstd151	human		GRCh37 chr11: 71,146,418-71,589,559 , GRCh38.p12 chr11: 71,435,372-71,878,513	, NADSYN1, 25 more genes

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Number of Variants: 20

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