OSC5991 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
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
nsv6630989	copy number variation	1	nstd224	human		GRCh37 chr6: 32,668,026-32,682,928 , GRCh38.p12 chr6: 32,700,249-32,715,151	MTCO3P1
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
nsv6627473	copy number variation	1	nstd224	human		GRCh37 chr22: 42,523,695-42,536,660 , GRCh38.p12 chr22\|NT_187682.1: 50,034-62,999	CYP2D7, CYP2D6, 1 more genes
nsv6621389	copy number variation	27	nstd224	human		GRCh37 chr12: 8,005,624-8,123,306 , GRCh38.p12 chr12: 7,853,028-7,970,710	SLC2A3, NANOGP1, 3 more genes
nsv6621551	copy number variation	1	nstd224	human		GRCh37 chr12: 124,115,018-124,194,438 , GRCh38.p12 chr12: 123,630,471-123,709,891	EIF2B1, TCTN2, 1 more genes
nsv6627380	copy number variation	480	nstd224	human		GRCh37 chr22: 24,374,253-24,390,432 , GRCh38.p12 chr22\|NT_187633.1: 268,428-284,607	GSTTP2, GSTT1-AS1, 2 more genes
nsv6633430	copy number variation	152	nstd224	human		GRCh37 chr9: 24,505,147-24,518,795 , GRCh38.p12 chr9: 24,505,149-24,518,797	0
nsv6623614	copy number variation	36	nstd224	human		GRCh37 chr16: 34,489,371-34,740,580 , GRCh38.p12 chr16: 35,255,000-35,506,209	LINC01566, AGGF1P9, 23 more genes
nsv6622002	copy number variation	111	nstd224	human		GRCh37 chr14: 20,198,662-20,417,653 , GRCh38.p12 chr14: 19,730,503-19,949,494	OR4N1P, OR4K3, 11 more genes
nsv6631893	copy number variation	2	nstd224	human		GRCh37 chr7: 43,748-63,494 , GRCh38.p12 chr7: 43,748-63,494 , GRCh38.p12 chr7\|NT_187558.1: 1-19,593 , GRCh38.p12 chr7\|NT_187653.1: 36,069-55,815	0

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