OSC4150 AND nstd224 - dbVar - NCBI

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Items: 10

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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
nsv6629498	copy number variation	31	nstd224	human		GRCh37 chr4: 58,055,260-58,094,886 , GRCh38.p12 chr4: 57,189,094-57,228,720	IGFBP7-AS1
nsv6633537	copy number variation	1	nstd224	human		GRCh37 chr9: 6,664,902-6,695,502 , GRCh38.p12 chr9: 6,664,902-6,695,502	RPL35AP20, RNF2P1
nsv6621232	copy number variation	5	nstd224	human		GRCh37 chr11: 95,569,448-95,621,376 , GRCh38.p12 chr11: 95,836,284-95,888,212	RNA5SP345, MTMR2
nsv6628116	copy number variation	277	nstd224	human		GRCh37 chr2: 38,956,836-38,972,328 , GRCh38.p12 chr2: 38,729,694-38,745,186	SRSF7, GALM
nsv6620631	copy number variation	3	nstd224	human		GRCh37 chr10: 47,543,322-47,662,471 , GRCh38.p12 chr10: 46,172,086-46,291,235	ANTXRLP1, AHCYP1, 2 more genes
nsv6622077	copy number variation	10	nstd224	human		GRCh37 chr13: 64,263,419-64,346,536 , GRCh38.p12 chr13: 63,689,286-63,772,403	OR7E156P, LINC00395, 2 more genes
nsv6626829	copy number variation	1	nstd224	human		GRCh37 chr20: 58,489,038-58,514,445 , GRCh38.p12 chr20: 59,913,983-59,939,390	FAM217B, PPP1R3D, 1 more genes
nsv6631445	copy number variation	586	nstd224	human		GRCh37 chr6: 67,017,543-67,044,431 , GRCh38.p12 chr6: 66,307,650-66,334,538	0
nsv6621601	copy number variation	56	nstd224	human		GRCh37 chr12: 31,296,219-31,406,907 , GRCh38.p12 chr12: 31,143,285-31,253,973 , GRCh38.p12 chr12\|NT_187587.1: 34,079-144,767	OVOS2, RPL13AP22, 5 more genes
nsv6622007	copy number variation	39	nstd224	human		GRCh37 chr14: 20,213,937-20,416,499 , GRCh38.p12 chr14: 19,745,778-19,948,340	OR4K4P, OR4H12P, 10 more genes

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