OSC6885 AND nstd224 - dbVar - NCBI

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Items: 12

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Number of Variants: 12

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
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
nsv6631959	copy number variation	1	nstd224	human		GRCh37 chr7: 470,316-506,206 , GRCh38.p12 chr7: 430,333-466,569	LOC112267991, LOC116435278
nsv6624960	copy number variation	42	nstd224	human		GRCh37 chr19: 41,355,925-41,387,391 , GRCh38.p12 chr19: 40,850,020-40,881,486	CYP2A7, CYP2A6
nsv6627442	copy number variation	2	nstd224	human		GRCh37 chr22: 25,731,297-25,911,465 , GRCh38.p12 chr22: 25,335,330-25,515,498	CRYBB2P1, LOC100419673, 2 more genes
nsv6625948	copy number variation	1	nstd224	human		GRCh37 chr1: 196,712,616-196,886,770 , GRCh38.p12 chr1: 196,743,486-196,917,640	CFH, CFHR1, 4 more genes
nsv6626924	copy number variation	21	nstd224	human		GRCh37 chr22: 24,302,227-24,402,531 , GRCh38.p12 chr22\|NT_187633.1: 196,402-296,706	GSTT1, GSTT2B, 10 more genes
nsv6632324	copy number variation	1	nstd224	human		GRCh37 chr8: 13,617,188-13,651,378 , GRCh38.p12 chr8: 13,759,679-13,793,869	0
nsv6623858	copy number variation	3	nstd224	human		GRCh37 chr17: 44,186,952-44,353,222 , GRCh38.p12 chr17: 46,109,586-46,275,856 , GRCh38.p12 chr17\|NT_187663.1: 811,685-954,783	KANSL1, KANSL1-AS1, 5 more genes
nsv6620305	copy number variation	1	nstd224	human		GRCh37 chr10: 105,154,089-105,294,641 , GRCh38.p12 chr10: 103,394,332-103,534,884	NEURL1, PDCD11, 6 more genes
nsv6631945	copy number variation	1	nstd224	human		GRCh37 chr7: 38,291,362-38,311,809 , GRCh38.p12 chr7: 38,251,761-38,272,208	TRG, TRGC1, 5 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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