dbVar for Gene (Select 120321) - 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
nsv5672640	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976	HSPD1P13, CARD17P, 239 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
nsv4980353	copy number variation	1	nstd200	human		GRCh38 chr11: 102,808,715-102,810,272 , GRCh37.p13 chr11: 102,679,446-102,681,003	WTAPP1, CSNK1A1P2
nsv4833608	copy number variation	1	nstd200	human		GRCh37 chr11: 102,679,446-102,681,003 , GRCh38.p12 chr11: 102,808,715-102,810,272	WTAPP1, CSNK1A1P2
nsv4712162	copy number variation	1	nstd195	human		GRCh37 chr11: 102,618,151-102,684,901 , GRCh38.p12 chr11: 102,747,420-102,814,170	MMP1, MMP10, 3 more genes
nsv4209193	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 102,679,446-102,681,003 , GRCh38.p12 chr11: 102,808,715-102,810,272	WTAPP1, CSNK1A1P2
nsv3924464	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 97,733,839-105,435,083 , GRCh38 chr11: 98,357,901-106,059,146 , GRCh37 chr11: 98,228,629-105,929,873	ARHGAP42, PDGFDDN, 91 more genes
nsv3922508	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 85,242,847-102,920,097 , GRCh37 chr11: 84,953,891-102,738,968 , NCBI36 chr11: 84,631,539-102,296,037	AMOTL1, LNCRNA-IUR, 240 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
nsv3915056	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 101,323,715-103,914,833 , NCBI36 chr11: 100,828,925-103,420,043 , GRCh38 chr11: 101,452,984-104,044,105	MMP27, MMP12, 47 more genes
nsv3913977	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 77,943,882-106,650,146 , GRCh38 chr11: 78,232,836-106,779,420 , NCBI36 chr11: 77,621,530-106,155,356	PLS1P1, SNORA25, 349 more genes
nsv3910663	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 91,086,659-109,595,582 , NCBI36 chr11: 90,459,475-108,971,518 , GRCh37 chr11: 90,819,827-109,466,308	LOC101060084, PGAM1P9, 230 more genes
nsv3910387	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr11: 101,948,892-102,308,304 , GRCh37.p13 chr11: 102,443,682-102,803,094 , GRCh38.p12 chr11: 102,572,951-102,932,365	MMP8, CSNK1A1P2, 11 more genes
nsv3910101	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 87,796,211-113,996,548 , GRCh37.p13 chr11: 88,156,563-114,491,338 , GRCh38.p12 chr11: 88,423,395-114,620,616	PHB1P16, LOC100418884, 385 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
nsv3908142	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 102,578,709-107,230,611 , GRCh38.p12 chr11: 102,707,978-107,359,885	CASP1, CASP4, 65 more genes
nsv3904761	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 80,053,454-113,316,236 , GRCh38.p12 chr11: 80,342,410-113,445,514	RPS6P16, CTSC, 449 more genes
nsv3901935	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 102,642,841-102,826,187 , GRCh38.p12 chr11: 102,772,110-102,955,458	MMP3, MMP12, 7 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
nsv3898361	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202	SESN3, LOC107984352, 694 more genes

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Number of Variants: 20

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Number of Variants: 20

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