OSC2561 AND nstd224 - dbVar - NCBI

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Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6630626	copy number variation	240	nstd224	human		GRCh37 chr5: 97,061,761-97,096,042 , GRCh38.p12 chr5: 97,726,057-97,760,338	LOC391813
nsv6622928	copy number variation	62	nstd224	human		GRCh37 chr15: 87,837,388-87,861,276 , GRCh38.p12 chr15: 87,294,157-87,318,045	LOC107984735
nsv6622933	copy number variation	37	nstd224	human		GRCh37 chr14: 99,182,535-99,193,023 , GRCh38.p12 chr14: 98,716,198-98,726,686	LINC02914
nsv6628914	copy number variation	179	nstd224	human		GRCh37 chr3: 173,259,356-173,289,281 , GRCh38.p12 chr3: 173,541,566-173,571,491	NLGN1
nsv6621668	copy number variation	1	nstd224	human		GRCh37 chr13: 20,797,144-21,118,721 , GRCh38.p12 chr13: 20,223,005-20,544,582	GJB6, CRYL1, 2 more genes
nsv6622984	copy number variation	38	nstd224	human		GRCh37 chr15: 24,357,212-24,472,278 , GRCh38.p12 chr15: 24,112,065-24,227,131	LOC105370732, PWRN2, 1 more genes
nsv6628034	copy number variation	50	nstd224	human		GRCh37 chr2: 242,917,734-243,020,723 , GRCh38.p12 chr2: 241,975,583-242,078,572 , GRCh38.p12 chr2\|NT_187523.1: 14,278-122,642 , GRCh38.p12 chr2\|NT_187647.1: 14,278-122,282	LINC01880, LINC01238, 3 more genes
nsv6627208	copy number variation	1	nstd224	human		GRCh37 chr22: 25,669,569-25,910,315 , GRCh38.p12 chr22: 25,273,602-25,514,348	CRYBB2P1, IGLL3P, 4 more genes
nsv6621457	copy number variation	226	nstd224	human		GRCh37 chr12: 31,266,287-31,406,907 , GRCh38.p12 chr12: 31,113,353-31,253,973 , GRCh38.p12 chr12\|NT_187587.1: 1,874-144,767	OVOS2, RPL13AP22, 6 more genes
nsv6620265	copy number variation	201	nstd224	human		GRCh37 chr10: 135,256,762-135,379,710 , GRCh38.p12 chr10: 133,443,258-133,566,206	CYP2E1, OR7M1P, 4 more genes
nsv6623615	copy number variation	320	nstd224	human		GRCh37 chr16: 34,516,075-34,686,820 , GRCh38.p12 chr16: 35,281,704-35,452,449	AGGF1P4, FRG2IP, 14 more genes

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OSC2561 AND nstd224 (12)
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