OSC7646 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
nsv6625091	copy number variation	291	nstd224	human		GRCh37 chr1: 110,228,505-110,241,385 , GRCh38.p12 chr1: 109,685,883-109,698,763	GSTM1
nsv6624477	copy number variation	2	nstd224	human		GRCh37 chr19: 41,349,732-41,380,418 , GRCh38.p12 chr19: 40,843,827-40,874,513	CYP2A6, CYP2A7
nsv6624685	copy number variation	256	nstd224	human		GRCh37 chr19: 20,605,360-20,700,135 , GRCh38.p12 chr19: 20,422,554-20,517,329	BNIP3P23, LOC105372317, 2 more genes
nsv6627551	copy number variation	1	nstd224	human		GRCh37 chr2: 214,052,437-214,647,339 , GRCh38.p12 chr2: 213,187,713-213,782,615	LOC107985981, SPAG16, 2 more genes
nsv6632533	copy number variation	3	nstd224	human		GRCh37 chr8: 2,132,549-2,393,044 , GRCh38.p12 chr8: 2,244,437-2,375,564 , GRCh38.p12 chr8\|NT_187576.1: 367,759-703,614	LOC105377782, LOC105377783, 3 more genes
nsv6625391	copy number variation	84	nstd224	human		GRCh37 chr1: 149,036,931-149,186,834 , GRCh38.p12 chr1: 143,542,264-143,692,183	NBPF17P, PFN1P12, 5 more genes
nsv6627053	copy number variation	7	nstd224	human		GRCh37 chr22: 22,318,346-22,563,845 , GRCh38.p12 chr22: 21,963,974-22,209,454	IGLVI-70, IGLVI-56, 24 more genes
nsv6631559	copy number variation	1	nstd224	human		GRCh37 chr7: 13,274,262-13,306,966 , GRCh38.p12 chr7: 13,234,637-13,267,341	0
nsv6628672	copy number variation	2	nstd224	human		GRCh37 chr3: 165,303,141-165,317,382 , GRCh38.p12 chr3: 165,585,353-165,599,594	0
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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OSC7646 AND nstd224 (11)
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