OSC6649 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
nsv6620207	copy number variation	3	nstd224	human		GRCh37 chr10: 23,062,951-23,107,911 , GRCh38.p12 chr10: 22,774,022-22,818,982	RNU6-413P
nsv6621982	copy number variation	1	nstd224	human		GRCh37 chr13: 93,131,369-93,145,448 , GRCh38.p12 chr13: 92,479,116-92,493,195	MIR548AS, GPC5
nsv6624780	copy number variation	3	nstd224	human		GRCh37 chr19: 53,320,646-53,344,919 , GRCh38.p12 chr19: 52,817,393-52,841,666	ZNF28, ZNF468
nsv6620570	copy number variation	2	nstd224	human		GRCh37 chr10: 47,536,152-47,654,624 , GRCh38.p12 chr10: 46,164,916-46,283,388	AHCYP1, ANTXRLP1, 1 more genes
nsv6622444	copy number variation	1	nstd224	human		GRCh37 chr14: 107,229,408-107,250,080 , GRCh38.p12 chr14: 106,821,177-106,841,864 , GRCh38.p12 chr14\|NT_187600.1: 1,312,351-1,333,038	IGHVIII-76-1, IGHV3-76, 3 more genes
nsv6627470	copy number variation	16	nstd224	human		GRCh37 chr22: 42,523,678-42,536,064 , GRCh38.p12 chr22\|NT_187682.1: 50,017-62,403	CYP2D6, CYP2D7, 1 more genes
nsv6625390	copy number variation	10	nstd224	human		GRCh37 chr1: 149,036,931-149,175,486 , GRCh38.p12 chr1: 143,542,264-143,680,846	NBPF17P, PFN1P12, 4 more genes
nsv6621014	copy number variation	1	nstd224	human		GRCh37 chr11: 67,501,626-67,727,252 , GRCh38.p12 chr11: 67,734,155-67,959,781	RPS3AP40, EVA1CP4, 10 more genes
nsv6633381	copy number variation	1	nstd224	human		GRCh37 chr9: 109,141,068-109,186,227 , GRCh38.p12 chr9: 106,378,787-106,423,946	0
nsv6632191	copy number variation	1	nstd224	human		GRCh37 chr7: 76,245,881-76,608,143 , GRCh38.p12 chr7: 76,616,564-76,978,826	POMZP3, FDPSP7, 4 more genes

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