OSC7150 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
nsv6625538	copy number variation	421	nstd224	human		GRCh37 chr1: 110,228,436-110,241,385 , GRCh38.p12 chr1: 109,685,814-109,698,763	GSTM1
nsv6627508	copy number variation	2	nstd224	human		GRCh37 chr2: 121,522,020-121,556,933 , GRCh38.p12 chr2: 120,764,444-120,799,357	GLI2
nsv6629951	copy number variation	36	nstd224	human		GRCh37 chr4: 69,401,172-69,435,325 , GRCh38.p12 chr4: 68,535,454-68,569,607	UGT2B17
nsv6623651	copy number variation	160	nstd224	human		GRCh37 chr16: 32,509,483-32,650,542 , GRCh38.p12 chr16: 32,498,162-32,639,221	FAM153DP, LOC107984013
nsv6630665	copy number variation	1	nstd224	human		GRCh37 chr6: 129,234,476-129,371,205 , GRCh38.p12 chr6: 128,913,331-129,050,060	LAMA2, MESTP1
nsv6628787	copy number variation	1	nstd224	human		GRCh37 chr3: 44,512,798-44,593,620 , GRCh38.p12 chr3: 44,471,306-44,552,128 , GRCh38.p12 chr3\|NW_009646197.1: 1-77,482	ZNF852, ZNF445, 3 more genes
nsv6625361	copy number variation	6	nstd224	human		GRCh37 chr1: 12,871,828-12,921,386 , GRCh38.p12 chr1: 12,811,688-12,861,531 , GRCh38.p12 chr1\|NW_012132914.1: 1-43,044	HNRNPCL1, LINC01784, 3 more genes
nsv6627470	copy number variation	16	nstd224	human		GRCh37 chr22: 42,523,678-42,536,064 , GRCh38.p12 chr22\|NT_187682.1: 50,017-62,403	CYP2D6, CYP2D7, 1 more genes
nsv6628364	copy number variation	27	nstd224	human		GRCh37 chr2: 89,504,808-90,241,820 , GRCh38.p12 chr2: 89,205,323-90,202,954	IGKV6D-41, IGKV3D-31, 52 more genes
nsv6622360	copy number variation	81	nstd224	human		GRCh37 chr14: 20,198,662-20,416,499 , GRCh38.p12 chr14: 19,730,503-19,948,340	OR4K6P, OR4K5, 11 more genes

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OSC7150 AND nstd224 (11)
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