OSC3013 AND nstd224 - dbVar - NCBI

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Items: 11

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Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6623961	copy number variation	1	nstd224	human		GRCh37 chr16: 76,768,372-76,844,155 , GRCh38.p12 chr16: 76,734,475-76,810,258	LOC105376774
nsv6620208	copy number variation	1	nstd224	human		GRCh37 chr10: 2,408,852-2,541,943 , GRCh38.p12 chr10: 2,366,658-2,499,751	LOC107983989, LINC02645
nsv6633598	copy number variation	154	nstd224	human		GRCh37 chr9: 140,173,637-140,196,334 , GRCh38.p12 chr9: 137,279,185-137,301,882	NRARP, TOR4A
nsv6624232	copy number variation	259	nstd224	human		GRCh37 chr17: 34,450,463-34,461,869 , GRCh38.p12 chr17: 36,123,077-36,134,487 , GRCh38.p12 chr17\|NT_187661.1: 77,174-88,584 , GRCh38.p12 chr17\|NT_187614.1: 357,991-369,397	LOC101927369, LOC107985055
nsv6628875	copy number variation	412	nstd224	human		GRCh37 chr3: 75,453,294-75,554,281 , GRCh38.p12 chr3: 75,404,143-75,505,130	ENPP7P2, LINC02018, 2 more genes
nsv6625656	copy number variation	1	nstd224	human		GRCh37 chr1: 1,597,351-1,663,831 , GRCh38.p12 chr1: 1,665,912-1,732,392	SLC35E2A, LOC100288379, 3 more genes
nsv6629065	copy number variation	500	nstd224	human		GRCh37 chr3: 65,193,246-65,211,507 , GRCh38.p12 chr3: 65,207,571-65,225,832	0
nsv6632192	copy number variation	4	nstd224	human		GRCh37 chr7: 76,414,540-76,639,871 , GRCh38.p12 chr7: 76,785,223-77,010,554	FDPSP7, DTX2P1-UPK3BP1-PMS2P11, 4 more genes
nsv6621306	copy number variation	2	nstd224	human		GRCh37 chr12: 11,213,998-11,244,602 , GRCh38.p12 chr12: 11,061,399-11,092,003	PRH1, TAS2R43, 4 more genes
nsv6622478	copy number variation	13	nstd224	human		GRCh37 chr14: 20,213,937-20,404,736 , GRCh38.p12 chr14: 19,745,778-19,936,577	OR4K6P, OR4K5, 10 more genes
nsv6622956	copy number variation	106	nstd224	human		GRCh37 chr15: 22,368,588-22,503,228 , GRCh38.p12 chr15: 22,080,637-22,215,277	IGHV1OR15-4, OR4N4, 9 more genes

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