dbVar for Gene (Select 105369473) - 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
nsv5918104	copy number variation	1	nstd209	human		GRCh38 chr11: 104,190,618-110,044,159 , GRCh37.p13 chr11: 104,061,346-109,914,884	, CARD18, 71 more genes
nsv5704599	mobile element insertion	2	nstd211	human		GRCh38 chr11: 106,113,558-106,113,558 , GRCh37.p13 chr11: 105,984,285-105,984,285	LINC02719
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
nsv5500656	copy number variation	1	nstd206	human		GRCh38 chr11: 106,106,909-106,112,995 , GRCh37.p13 chr11: 105,977,636-105,983,722	LINC02719
nsv5401048	mobile element insertion	1	nstd206	human		GRCh38 chr11: 106,113,558-106,113,609 , GRCh37.p13 chr11: 105,984,285-105,984,336	LINC02719
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
nsv4706973	copy number variation	1	nstd195	human		GRCh37 chr11: 105,829,401-105,993,301 , GRCh38.p12 chr11: 105,958,674-106,122,574	GRIA4, AASDHPPT, 4 more genes
nsv4705616	copy number variation	1	nstd195	human		GRCh37 chr11: 105,995,401-106,205,251 , GRCh38.p12 chr11: 106,124,674-106,334,524	LOC643855, LOC101928535, 1 more genes
nsv4676052	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 103,980,525-106,914,369 , GRCh38.p12 chr11: 104,109,797-107,043,643	CARD17P, LOC643855, 36 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
nsv4675179	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 105,875,295-106,313,332 , GRCh38.p12 chr11: 106,004,568-106,442,605	LOC643855, MSANTD4, 5 more genes
nsv4675055	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 103,983,847-106,914,369 , GRCh38.p12 chr11: 104,113,119-107,043,643	LOC105369466, CASP4LP, 36 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
nsv4455453	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 105,875,296-106,210,917 , GRCh38.p12 chr11: 106,004,569-106,340,190	LOC101928535, AASDHPPT, 4 more genes
nsv4212345	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 105,885,000-106,313,400 , GRCh38.p12 chr11: 106,014,273-106,442,673	AASDHPPT, MSANTD4, 5 more genes
nsv4206513	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 106,001,970-106,006,667 , GRCh38.p12 chr11: 106,131,243-106,135,940	LINC02719
nsv4194031	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 105,977,636-105,983,722 , GRCh38.p12 chr11: 106,106,909-106,112,995	LINC02719
nsv3962367	copy number variation	1	nstd168	human		GRCh38 chr11: 106,101,424-106,121,849 , GRCh37.p13 chr11: 105,972,151-105,992,576	LINC02719
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

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Number of Variants: 20

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Items: 1 to 20 of 129

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Number of Variants: 20

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