OSC5907 AND nstd224 - dbVar - NCBI

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Number of Variants: 10

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6629898	copy number variation	832	nstd224	human		GRCh37 chr4: 69,401,172-69,435,811 , GRCh38.p12 chr4: 68,535,454-68,570,093	UGT2B17
nsv6630032	copy number variation	2	nstd224	human		GRCh37 chr5: 114,709,028-114,719,148 , GRCh38.p12 chr5: 115,373,331-115,383,451	LOC105379130
nsv6634108	copy number variation	11	nstd224	human		GRCh37 chrX: 94,314,391-94,375,989 , GRCh38.p12 chrX: 95,059,392-95,120,990	MIR548M
nsv6631956	copy number variation	2	nstd224	human		GRCh37 chr7: 43,748-68,891 , GRCh38.p12 chr7: 43,748-68,891 , GRCh38.p12 chr7\|NT_187558.1: 1-24,990 , GRCh38.p12 chr7\|NT_187653.1: 36,069-61,212	LOC105375113
nsv6623896	copy number variation	1	nstd224	human		GRCh37 chr16: 74,828,378-74,937,650 , GRCh38.p12 chr16: 74,794,480-74,903,752	WDR59, LOC105371343
nsv6633729	copy number variation	1	nstd224	human		GRCh37 chr9: 25,555,386-25,627,885 , GRCh38.p12 chr9: 25,555,388-25,627,887	LOC105375997, LOC105375996
nsv6632862	copy number variation	1	nstd224	human		GRCh37 chr9: 105,868,318-105,940,438 , GRCh38.p12 chr9: 103,106,036-103,178,156	LOC105376191, LINC01492
nsv6625780	copy number variation	1	nstd224	human		GRCh37 chr1: 157,931,997-158,060,178 , GRCh38.p12 chr1: 157,962,207-158,090,388	KIRREL1, KIRREL1-IT1, 1 more genes
nsv6625898	copy number variation	2	nstd224	human		GRCh37 chr1: 161,524,096-161,616,504 , GRCh38.p12 chr1: 161,554,306-161,646,714	FCGR2B, FCGR3B, 4 more genes
nsv6622362	copy number variation	29	nstd224	human		GRCh37 chr14: 20,198,833-20,416,499 , GRCh38.p12 chr14: 19,730,674-19,948,340	OR4K6P, OR4K5, 11 more genes

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