OSC4823 AND nstd224 - dbVar - NCBI

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Number of Variants: 10

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6629478	copy number variation	1	nstd224	human		GRCh37 chr4: 27,216,501-27,298,305 , GRCh38.p12 chr4: 27,214,879-27,296,683	LINC02261
nsv6632491	copy number variation	2	nstd224	human		GRCh37 chr8: 135,622,851-135,771,896 , GRCh38.p12 chr8: 134,610,608-134,759,653	ZFAT
nsv6628794	copy number variation	1	nstd224	human		GRCh37 chr3: 58,844,331-58,970,958 , GRCh38.p12 chr3: 58,858,605-58,985,232	CFAP20DC-AS1, CFAP20DC
nsv6626074	copy number variation	11	nstd224	human		GRCh37 chr1: 196,801,025-196,887,530 , GRCh38.p12 chr1: 196,831,895-196,918,400	CFHR1, CFHR4, 2 more genes
nsv6624278	copy number variation	1	nstd224	human		GRCh37 chr17: 4,375,507-4,453,485 , GRCh38.p12 chr17: 4,472,212-4,550,190	SPNS2, SPNS2-AS1, 2 more genes
nsv6623954	copy number variation	4	nstd224	human		GRCh37 chr16: 75,539,436-75,575,997 , GRCh38.p12 chr16: 75,505,538-75,542,099	CHST5, TMEM231, 1 more genes
nsv6633920	copy number variation	98	nstd224	human		GRCh37 chr9: 5,306,824-5,335,570 , GRCh38.p12 chr9: 5,306,824-5,335,570	RLN1, RLN2, 1 more genes
nsv6625130	copy number variation	188	nstd224	human		GRCh37 chr19: 43,344,686-43,528,980 , GRCh38.p12 chr19: 42,840,534-43,024,828	CEACAMP7, PSG1, 4 more genes
nsv6622369	copy number variation	248	nstd224	human		GRCh37 chr14: 20,213,937-20,420,151 , GRCh38.p12 chr14: 19,745,778-19,951,992	OR4N1P, OR4K1, 10 more genes
nsv6632147	copy number variation	132	nstd224	human		GRCh37 chr7: 44,935-67,365 , GRCh38.p12 chr7: 44,935-67,365 , GRCh38.p12 chr7\|NT_187558.1: 1,034-23,464 , GRCh38.p12 chr7\|NT_187653.1: 37,256-59,686	0

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