dbVar for Gene (Select 100302240) - 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
nsv5497804	copy number variation	1	nstd206	human		GRCh38 chr11: 93,482,000-94,038,896 , GRCh37.p13 chr11: 93,215,166-93,772,062	SNORA1, HPRT1P3, 20 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
nsv4989177	copy number variation	1	nstd200	human		GRCh38 chr11: 93,732,971-93,738,972 , GRCh37.p13 chr11: 93,466,137-93,472,138	SNORA40, SNORD5, 4 more genes
nsv4989175	copy number variation	1	nstd200	human		GRCh38 chr11: 93,501,300-93,857,533 , GRCh37.p13 chr11: 93,234,466-93,590,699	VSTM5, SNORA18, 17 more genes
nsv4971591	copy number variation	1	nstd200	human		GRCh38 chr11: 91,285,470-94,799,390 , GRCh37.p13 chr11: 91,018,638-94,532,556	, LOC105369429, 53 more genes
nsv4839969	copy number variation	1	nstd200	human		GRCh37 chr11: 91,018,638-94,532,556 , GRCh38.p12 chr11: 91,285,470-94,799,390	, MIR548L, 53 more genes
nsv4729052	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 92,615,227-93,592,229 , GRCh38.p12 chr11: 92,882,061-93,859,063	CEP295, RPL26P31, 26 more genes
nsv4675146	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 93,297,444-94,041,273 , GRCh38.p12 chr11: 93,564,278-94,308,107	SCARNA9, SNORD5, 22 more genes
nsv4616044	copy number variation	1	nstd183	human		GRCh37 chr11: 93,319,098-93,964,452 , GRCh38.p12 chr11: 93,585,932-94,231,286	TAF1D, SNORD6, 21 more genes
nsv3923008	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr11: 92,985,144-93,113,871 , GRCh37.p13 chr11: 93,345,496-93,474,223 , GRCh38.p12 chr11: 93,612,330-93,741,057	SNORA8, CEP295, 11 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
nsv3921121	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 75,941,754-98,357,960 , NCBI36 chr11: 75,330,446-97,733,898 , GRCh37 chr11: 75,652,798-98,228,688	LOC105369441, RNU6-1135P, 296 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
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
nsv3906008	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 83,179,196-94,716,998 , GRCh38.p12 chr11: 83,468,153-94,983,834	SNORA18, PIWIL4, 157 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

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Number of Variants: 20

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Result Filters

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Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 86

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Number of Variants: 20

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