OSC6755 AND nstd224 - dbVar - NCBI

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Items: 11

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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
nsv6625934	copy number variation	39	nstd224	human		GRCh37 chr1: 189,332,108-189,539,782 , GRCh38.p12 chr1: 189,362,978-189,570,652	LOC105371657
nsv6627352	copy number variation	3	nstd224	human		GRCh37 chr2: 153,670,186-153,797,204 , GRCh38.p12 chr2: 152,813,672-152,940,690	UBQLN4P2
nsv6623110	copy number variation	2	nstd224	human		GRCh37 chr15: 39,520,813-39,589,246 , GRCh38.p12 chr15: 39,228,612-39,297,045	LINC02915
nsv6629958	copy number variation	5	nstd224	human		GRCh37 chr4: 69,409,792-69,427,232 , GRCh38.p12 chr4: 68,544,074-68,561,514	UGT2B17
nsv6624715	copy number variation	13	nstd224	human		GRCh37 chr19: 41,349,596-41,381,212 , GRCh38.p12 chr19: 40,843,691-40,875,307	CYP2A7, CYP2A6
nsv6623656	copy number variation	24	nstd224	human		GRCh37 chr16: 32,523,490-32,650,542 , GRCh38.p12 chr16: 32,512,169-32,639,221	LOC107984013, FAM153DP
nsv6625340	copy number variation	7	nstd224	human		GRCh37 chr1: 106,043,271-106,259,935 , GRCh38.p12 chr1: 105,500,649-105,717,313	LINC01676, SEPTIN2P1, 1 more genes
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
nsv6627381	copy number variation	27	nstd224	human		GRCh37 chr22: 24,374,253-24,402,531 , GRCh38.p12 chr22\|NT_187633.1: 268,428-296,706	GSTT1-AS1, GSTTP2, 2 more genes
nsv6624231	copy number variation	76	nstd224	human		GRCh37 chr17: 34,438,753-34,476,927 , GRCh38.p12 chr17: 36,111,360-36,149,545 , GRCh38.p12 chr17\|NT_187661.1: 65,457-103,642 , GRCh38.p12 chr17\|NT_187614.1: 346,281-384,455	LOC107985055, LOC101927369, 1 more genes
nsv6621424	copy number variation	1	nstd224	human		GRCh37 chr12: 132,063,158-132,189,391 , GRCh38.p12 chr12: 131,578,613-131,704,846	RPS6P21, LOC100996701, 5 more genes

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