OSC3391 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
nsv6625378	copy number variation	31	nstd224	human		GRCh37 chr1: 1,386,089-1,431,163 , GRCh38.p12 chr1: 1,450,709-1,495,783	ATAD3C, ATAD3B
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
nsv6625472	copy number variation	64	nstd224	human		GRCh37 chr1: 104,113,158-104,128,618 , GRCh38.p12 chr1: 103,570,536-103,585,996	AMY2B, ACTG1P4
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
nsv6625811	copy number variation	25	nstd224	human		GRCh37 chr1: 17,216,331-17,273,287 , GRCh38.p12 chr1: 16,889,836-16,946,792	TRN-GTT4-1, LOC105376805, 3 more genes
nsv6632011	copy number variation	1	nstd224	human		GRCh37 chr7: 76,144,403-76,637,441 , GRCh38.p12 chr7: 76,515,086-77,008,124	POMZP3, FDPSP7, 7 more genes
nsv6631282	copy number variation	9	nstd224	human		GRCh37 chr6: 95,502,730-95,556,864 , GRCh38.p12 chr6: 94,793,012-94,847,146	0
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
nsv6621457	copy number variation	226	nstd224	human		GRCh37 chr12: 31,266,287-31,406,907 , GRCh38.p12 chr12: 31,113,353-31,253,973 , GRCh38.p12 chr12\|NT_187587.1: 1,874-144,767	OVOS2, RPL13AP22, 6 more genes
nsv6633963	copy number variation	1	nstd224	human		GRCh37 chrX: 118,763,453-119,037,260 , GRCh38.p12 chrX: 119,629,490-119,903,297	RPL39, LOC100422368, 9 more genes

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