OSC3021 AND nstd224 - dbVar - NCBI

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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
nsv6628195	copy number variation	1	nstd224	human		GRCh37 chr3: 11,552,027-11,710,471 , GRCh38.p12 chr3: 11,510,553-11,668,997	ATG7, VGLL4
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
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
nsv6625918	copy number variation	16	nstd224	human		GRCh37 chr1: 17,216,331-17,270,614 , GRCh38.p12 chr1: 16,889,836-16,944,119	CROCC, LOC105376805, 3 more genes
nsv6628296	copy number variation	1	nstd224	human		GRCh37 chr2: 39,583,431-39,789,288 , GRCh38.p12 chr2: 39,356,290-39,562,147	MAP4K3, RNU6-1341P, 1 more genes
nsv6632900	copy number variation	1	nstd224	human		GRCh37 chr8: 67,900,620-68,004,117 , GRCh38.p12 chr8: 66,988,385-67,091,882	CSPP1, PPP1R42, 2 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
nsv6628234	copy number variation	32	nstd224	human		GRCh37 chr2: 89,442,329-90,248,974 , GRCh38.p12 chr2: 89,142,846-90,210,108	ABCD1P1, IGKV3D-15, 60 more genes
nsv6622634	copy number variation	2	nstd224	human		GRCh37 chr14: 38,958,967-39,041,292 , GRCh38.p12 chr14: 38,489,763-38,572,088	0
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
nsv6627184	copy number variation	1	nstd224	human		GRCh37 chr22: 21,799,719-23,803,722 , GRCh38.p12 chr22: 21,445,430-23,461,535	BCRP4, GNAZ, 158 more genes

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OSC3021 AND nstd224 (12)
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