dbVar for Gene (Select 30819) - 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
nsv5910193	copy number variation	1	nstd209	human		GRCh38 chr10: 101,836,818-101,836,985 , GRCh37.p13 chr10: 103,596,575-103,596,742	KCNIP2
nsv4973985	copy number variation	1	nstd200	human		GRCh38 chr10: 101,791,930-101,838,328 , GRCh37.p13 chr10: 103,551,687-103,598,085	OGA, KCNIP2-AS1, 1 more genes
nsv4837880	copy number variation	1	nstd200	human		GRCh37 chr10: 103,551,687-103,598,085 , GRCh38.p12 chr10: 101,791,930-101,838,328	OGA, KCNIP2-AS1, 1 more genes
nsv4728795	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 103,582,453-103,931,269 , GRCh38.p12 chr10: 101,822,696-102,171,512	HPS6, NOLC1, 6 more genes
nsv4680797	copy number variation	1	nstd189	human		GRCh37.p13 chr10: 102,835,750-103,653,301 , GRCh38.p12 chr10: 101,075,993-101,893,544	, FGF8, 28 more genes
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
nsv3969704	insertion	1	nstd168	human		GRCh38 chr10: 101,840,534-101,880,229 , GRCh37.p13 chr10: 103,600,291-103,639,986	, KCNIP2, 2 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
nsv3917824	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 102,880,104-103,591,665 , NCBI36 chr10: 102,870,094-103,581,655 , GRCh38 chr10: 101,120,347-101,831,908	KCNIP2-AS1, RNU2-59P, 23 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
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
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
nsv3894450	copy number variation	1	nstd102	human	drug response	GRCh37 chr10: 85,557,432-105,804,295 , GRCh38.p12 chr10: 83,797,676-104,044,537	HPS1, LOC112268063, 422 more genes

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Items: 1 to 20 of 98

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Number of Variants: 20

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