dbVar for Gene (Select 119392) - 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
nsv4728834	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 105,839,235-105,890,455 , GRCh38.p12 chr10: 104,079,477-104,130,697	CFAP43, SFR1, 1 more genes
nsv4605011	copy number variation	1	nstd183	human		GRCh37 chr10: 105,881,710-105,891,455 , GRCh38.p12 chr10: 104,121,952-104,131,697	CFAP43, SFR1
nsv4599751	copy number variation	1	nstd183	human		GRCh37 chr10: 105,881,698-105,883,474 , GRCh38.p12 chr10: 104,121,940-104,123,716	SFR1
nsv4527651	copy number variation	1	nstd166	human		GRCh37.p13 chr10: 105,880,247-105,880,866 , GRCh38.p12 chr10: 104,120,489-104,121,108	SFR1
nsv4339713	sequence alteration	1	nstd166	human		GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970	, ADRA2A, 1651 more genes
nsv4325673	inversion	1	nstd166	human		GRCh37.p13 chr10: 92,228,734-107,785,320 , GRCh38.p12 chr10: 90,468,977-106,025,562	, COX15, 323 more genes
nsv3923769	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 100,194,215-132,432,797 , GRCh37 chr10: 101,953,972-134,246,301 , NCBI36 chr10: 101,943,962-134,096,291	LOC105378493, LINC02627, 477 more genes
nsv3922274	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr10: 103,274,160-135,374,737 , GRCh37.p13 chr10: 103,284,170-135,524,747 , GRCh38.p12 chr10: 101,524,413-133,787,422	DPCD, LOC105378467, 504 more genes
nsv3921919	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 100,600,492-133,622,588 , GRCh37 chr10: 102,360,249-135,436,092 , NCBI36 chr10: 102,350,239-135,286,082	MIR4295, BORCS7, 508 more genes
nsv3920295	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422	EIF2S2P3, CYP17A1-AS1, 895 more genes
nsv3920131	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr10: 104,077,161-108,350,985 , NCBI36 chr10: 105,826,909-110,100,733 , GRCh37 chr10: 105,836,919-110,110,743	SORCS1, LOC105378469, 37 more genes
nsv3916477	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 104,481,920-115,834,854 , GRCh37 chr10: 104,491,930-115,844,864 , GRCh38 chr10: 102,732,173-114,085,105	XPNPEP1, NRAP, 147 more genes
nsv3909942	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 96,872,364-118,383,651 , GRCh38 chr10: 95,112,607-116,776,637 , NCBI36 chr10: 96,862,354-118,526,138	LOC102723665, SFR1, 360 more genes
nsv3907664	copy number variation	1	nstd102	human	drug response	GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422	SHOC2, FAM245B, 1487 more genes
nsv3906389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996	LOC100419870, LOC102724439, 2105 more genes
nsv3905499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 104,030,479-115,410,590 , GRCh38.p12 chr10: 102,270,722-113,650,831	RPS15AP30, PDCD11, 156 more genes
nsv3905489	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,283,493-135,427,143 , GRCh38.p12 chr10: 91,523,736-133,613,639	LOC105378476, SMC3, 688 more genes
nsv3903027	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 105,613,040-135,427,143 , GRCh38.p12 chr10: 103,853,282-133,613,639	YWHAZP5, LOC102724883, 415 more genes
nsv3902271	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639	ANXA11, EDRF1-DT, 2085 more genes
nsv3898332	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 103,288,313-135,512,075 , GRCh38.p12 chr10: 101,528,556-133,774,750	NPS, BTF3P15, 503 more genes

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Number of Variants: 20

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Number of Variants: 20

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