OSC6461 AND nstd224 - dbVar - NCBI

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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
nsv6626109	copy number variation	1	nstd224	human		GRCh37 chr1: 237,538,093-237,591,215 , GRCh38.p12 chr1: 237,374,793-237,427,915	RYR2
nsv6630814	copy number variation	62	nstd224	human		GRCh37 chr5: 97,051,856-97,096,042 , GRCh38.p12 chr5: 97,716,152-97,760,338	LOC391813
nsv6625538	copy number variation	421	nstd224	human		GRCh37 chr1: 110,228,436-110,241,385 , GRCh38.p12 chr1: 109,685,814-109,698,763	GSTM1
nsv6628003	copy number variation	118	nstd224	human		GRCh37 chr2: 228,241,621-228,258,199 , GRCh38.p12 chr2: 227,376,905-227,393,483	TM4SF20
nsv6631843	copy number variation	45	nstd224	human		GRCh37 chr7: 142,835,239-142,881,540 , GRCh38.p12 chr7: 143,138,146-143,184,447	PIP, TAS2R39
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
nsv6630470	copy number variation	1	nstd224	human		GRCh37 chr5: 12,544,407-12,573,166 , GRCh38.p12 chr5: 12,544,295-12,573,054	LINC01194, LOC105374655
nsv6620861	copy number variation	1	nstd224	human		GRCh37 chr10: 92,086,724-92,576,260 , GRCh38.p12 chr10: 90,326,967-90,816,503	LINC02653, HTR7
nsv6626369	copy number variation	153	nstd224	human		GRCh37 chr1: 25,604,951-25,655,563 , GRCh38.p12 chr1: 25,278,460-25,329,072	RSRP1, RHD, 1 more genes
nsv6621456	copy number variation	4	nstd224	human		GRCh37 chr12: 31,266,287-31,383,052 , GRCh38.p12 chr12: 31,113,353-31,230,118 , GRCh38.p12 chr12\|NT_187587.1: 1,874-120,912	OVOS2, LOC101060058, 1 more genes
nsv6624084	copy number variation	158	nstd224	human		GRCh37 chr17: 44,179,983-44,353,222 , GRCh38.p12 chr17: 46,102,617-46,275,856 , GRCh38.p12 chr17\|NT_187663.1: 804,722-954,783	KANSL1, KANSL1-AS1, 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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