dbVar for Gene (Select 1586) - 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
nsv5507325	copy number variation	1	nstd206	human		GRCh38 chr10: 102,828,010-102,828,753 , GRCh37.p13 chr10: 104,587,767-104,588,510	CYP17A1
nsv4829703	copy number variation	1	nstd200	human		GRCh37 chr10: 104,588,780-104,589,587 , GRCh38.p12 chr10: 102,829,023-102,829,830	CYP17A1
nsv4679283	copy number variation	1	nstd189	human		GRCh37.p13 chr10: 104,468,424-105,156,097 , GRCh38.p12 chr10: 102,708,667-103,396,340	, ARL3, 25 more genes
nsv4389533	copy number variation	1	nstd171	human		GRCh37 chr10: 104,590,837-104,590,871 , GRCh38.p12 chr10: 102,831,080-102,831,114	CYP17A1, CYP17A1-AS1
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
nsv4191024	copy number variation	1	nstd166	human		GRCh37.p13 chr10: 104,593,910-104,608,284 , GRCh38.p12 chr10: 102,834,153-102,848,527	, CYP17A1-AS1, 3 more genes
nsv3941947	copy number variation	1	nstd167	human		GRCh37 chr10: 104,590,836-104,590,871 , GRCh38.p12 chr10: 102,831,079-102,831,114	CYP17A1, CYP17A1-AS1
nsv3924696	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 102,243,341-103,929,730 , GRCh37 chr10: 104,003,098-105,689,488 , NCBI36 chr10: 103,993,088-105,679,478	MIR146B, RPL23AP58, 48 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
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
nsv3912564	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr10: 102,710,547-103,110,626 , GRCh37 chr10: 104,470,304-104,870,383 , NCBI36 chr10: 104,460,294-104,860,373	SFXN2, RNU6-1231P, 13 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

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Number of Variants: 20

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