dbVar for Gene (Select 407042) - 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
nsv5509179	copy number variation	1	nstd206	human		GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687	, ATM, 153 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
nsv4989298	copy number variation	1	nstd200	human		GRCh38 chr11: 111,496,095-111,534,266 , GRCh37.p13 chr11: 111,366,820-111,404,991	BTG4, MIR34C, 3 more genes
nsv4683939	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr11: 111,171,709-111,965,694 , GRCh38.p12 chr11: 111,300,984-112,094,970	FDXACB1, LOC107984386, 34 more genes
nsv4675680	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 103,320,065-114,349,787 , GRCh38.p12 chr11: 103,449,337-114,479,065	DRD2, NCAM1, 181 more genes
nsv4675323	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 105,699,599-114,524,876 , GRCh38.p12 chr11: 105,828,873-114,654,154	RPSAP50, RNA5SP349, 155 more genes
nsv4456659	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 110,969,076-114,578,509 , GRCh38.p12 chr11: 111,098,352-114,707,787	RPS29P19, PPP2R1B, 95 more genes
nsv4455554	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 104,101,411-116,680,918 , GRCh38.p12 chr11: 104,230,683-116,810,202	LINC02732, LINC02698, 198 more genes
nsv4200622	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 111,366,820-111,404,991 , GRCh38.p12 chr11: 111,496,095-111,534,266	MIR34BHG, MIR34B, 3 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
nsv3913577	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 105,972,805-113,384,939 , GRCh37.p13 chr11: 106,467,595-113,879,729 , GRCh38.p12 chr11: 106,596,868-114,009,007	LAYN, DDX10, 133 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
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
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
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
nsv3139652	copy number variation	1	nstd151	human		GRCh37 chr11: 110,007,386-113,570,418 , GRCh38.p12 chr11: 110,136,661-113,699,696	, DRD2, 82 more genes
nsv2733261	copy number variation	1	nstd130	human		NCBI36 chr11: 102,890,408-111,465,743 , GRCh37.p13 chr11: 103,385,198-111,960,533 , GRCh38.p12 chr11: 103,514,470-112,089,809	, DDI1, 130 more genes

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Number of Variants: 20

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 84

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Number of Variants: 20

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