OSC2590 AND nstd224 - dbVar - NCBI

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6626823	copy number variation	64	nstd224	human		GRCh37 chr20: 58,440,438-58,496,439 , GRCh38.p12 chr20: 59,865,383-59,921,384	SYCP2
nsv6620904	copy number variation	1	nstd224	human		GRCh37 chr11: 17,313,521-17,369,517 , GRCh38.p12 chr11: 17,291,974-17,347,970	NUCB2
nsv6622673	copy number variation	3	nstd224	human		GRCh37 chr14: 60,903,572-60,936,278 , GRCh38.p12 chr14: 60,436,854-60,469,560	C14orf39
nsv6634281	copy number variation	1	nstd224	human		GRCh37 chrX: 83,116,204-83,141,579 , GRCh38.p12 chrX: 83,861,196-83,886,571	CYLC1
nsv6622122	copy number variation	288	nstd224	human		GRCh37 chr13: 21,729,252-21,746,637 , GRCh38.p12 chr13: 21,155,113-21,172,498	SKA3
nsv6620878	copy number variation	140	nstd224	human		GRCh37 chr11: 107,653,081-107,670,228 , GRCh38.p12 chr11: 107,782,355-107,799,502	SLC35F2
nsv6632510	copy number variation	2	nstd224	human		GRCh37 chr8: 144,984,956-144,999,874 , GRCh38.p12 chr8: 143,910,788-143,925,706	PLEC
nsv6620858	copy number variation	1	nstd224	human		GRCh37 chr10: 91,487,648-91,498,175 , GRCh38.p12 chr10: 89,727,891-89,738,418	KIF20B
nsv6633699	copy number variation	1	nstd224	human		GRCh37 chr9: 17,415,825-17,464,622 , GRCh38.p12 chr9: 17,415,827-17,464,624	SAMM50P1, CNTLN
nsv6628926	copy number variation	1	nstd224	human		GRCh37 chr3: 184,184,235-184,232,464 , GRCh38.p12 chr3: 184,466,447-184,514,676 , GRCh38.p12 chr3\|NT_187538.1: 18,663-66,892	LINC01839, TEDDM3P
nsv6632914	copy number variation	25	nstd224	human		GRCh37 chr8: 8,094,406-8,132,754 , GRCh38.p12 chr8: 8,236,884-8,275,232 , GRCh38.p12 chr8\|NW_018654717.1: 5,072,622-5,110,981	FAM86B3P, ALG1L13P
nsv6625922	copy number variation	1	nstd224	human		GRCh37 chr1: 17,594,365-17,607,292 , GRCh38.p12 chr1: 17,267,870-17,280,797 , GRCh38.p12 chr1\|NW_011332688.1: 110,384-123,311	MIR3972, PADI3
nsv6624844	copy number variation	645	nstd224	human		GRCh37 chr19: 20,630,360-20,715,228 , GRCh38.p12 chr19: 20,447,554-20,532,422	ZNF737, LOC105372316, 1 more genes
nsv6633226	copy number variation	78	nstd224	human		GRCh37 chr9: 140,166,981-140,196,334 , GRCh38.p12 chr9: 137,272,529-137,301,882	NRARP, TOR4A, 1 more genes
nsv6632397	copy number variation	1	nstd224	human		GRCh37 chr7: 85,990,367-86,107,652 , GRCh38.p12 chr7: 86,361,051-86,478,336	0
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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