OSC8265 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
nsv6629956	copy number variation	1	nstd224	human		GRCh37 chr4: 69,409,246-69,435,242 , GRCh38.p12 chr4: 68,543,528-68,569,524	UGT2B17
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
nsv6624319	copy number variation	1	nstd224	human		GRCh37 chr17: 78,224,113-78,319,385 , GRCh38.p12 chr17: 80,250,314-80,345,585	RNF213, SLC26A11
nsv6620263	copy number variation	26	nstd224	human		GRCh37 chr10: 135,252,932-135,376,669 , GRCh38.p12 chr10: 133,439,428-133,563,165	CYP2E1, SYCE1, 3 more genes
nsv6632795	copy number variation	8	nstd224	human		GRCh37 chr8: 2,133,338-2,393,044 , GRCh38.p12 chr8: 2,244,437-2,375,564 , GRCh38.p12 chr8\|NT_187576.1: 368,548-703,614	LINC03021, LOC105377783, 3 more genes
nsv6634207	copy number variation	6	nstd224	human		GRCh37 chrX: 134,756,293-134,911,512 , GRCh38.p12 chrX: 135,622,368-135,743,081	SAGE4P, SAGE2P, 3 more genes
nsv6625349	copy number variation	3	nstd224	human		GRCh37 chr1: 12,832,317-13,634,781 , GRCh38.p12 chr1: 12,772,175-13,308,389	PRAMEF13, PRAMEF6, 30 more genes
nsv6620628	copy number variation	93	nstd224	human		GRCh37 chr10: 47,146,867-47,703,869 , GRCh38.p12 chr10: 46,157,935-47,739,149	GDF10, RBP3, 48 more genes
nsv6628416	copy number variation	2	nstd224	human		GRCh37 chr2: 87,394,756-87,833,685 , GRCh38.p12 chr2: 87,167,633-87,534,166	CENPNP1, LOC100652743, 10 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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