OSC6691 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
nsv6632493	copy number variation	72	nstd224	human		GRCh37 chr8: 137,688,230-137,855,721 , GRCh38.p12 chr8: 136,675,987-136,843,478	LINC02055
nsv6620658	copy number variation	1	nstd224	human		GRCh37 chr10: 68,079,310-68,117,739 , GRCh38.p12 chr10: 66,319,552-66,357,981	CTNNA3
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
nsv6624121	copy number variation	1	nstd224	human		GRCh37 chr17: 78,087,041-78,098,477 , GRCh38.p12 chr17: 80,113,242-80,124,678	GAA
nsv6625487	copy number variation	38	nstd224	human		GRCh37 chr1: 110,228,436-110,243,335 , GRCh38.p12 chr1: 109,685,814-109,700,713	GSTM1
nsv6622458	copy number variation	32	nstd224	human		GRCh37 chr14: 21,357,547-21,411,866 , GRCh38.p12 chr14: 20,889,388-20,943,707	RNASE2CP, RNASE3, 1 more genes
nsv6633913	copy number variation	15	nstd224	human		GRCh37 chr9: 43,393,590-43,428,145 , GRCh38.p12 chr9: 42,383,725-42,418,560	ATP5F1AP1, FKBP4P6, 1 more genes
nsv6625564	copy number variation	3	nstd224	human		GRCh37 chr1: 12,855,789-12,948,317 , GRCh38.p12 chr1: 12,795,640-12,888,493	PRAMEF1, PRAMEF2, 5 more genes
nsv6623220	copy number variation	151	nstd224	human		GRCh37 chr16: 34,489,371-34,724,788 , GRCh38.p12 chr16: 35,255,000-35,490,417	AGGF1P4, C2orf69P3, 21 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
nsv6627200	copy number variation	37	nstd224	human		GRCh37 chr22: 24,302,601-24,390,432 , GRCh38.p12 chr22\|NT_187633.1: 196,776-284,607	GSTT1, GSTT2B, 10 more genes

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