OSC5724 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
nsv6626833	copy number variation	3	nstd224	human		GRCh37 chr20: 62,193,253-62,203,708 , GRCh38.p12 chr20: 63,561,900-63,572,355	HELZ2
nsv6632760	copy number variation	2	nstd224	human		GRCh37 chr8: 144,943,389-145,003,862 , GRCh38.p12 chr8: 143,869,221-143,929,694	PLEC, EPPK1
nsv6628018	copy number variation	15	nstd224	human		GRCh37 chr2: 239,038,829-239,049,729 , GRCh38.p12 chr2: 238,130,188-238,141,088	ESPNL, KLHL30
nsv6629785	copy number variation	1	nstd224	human		GRCh37 chr4: 81,283,923-81,554,785 , GRCh38.p12 chr4: 80,362,769-80,633,631	LOC100419739, LOC105377305, 1 more genes
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
nsv6626486	copy number variation	1	nstd224	human		GRCh37 chr1: 934,735-977,396 , GRCh38.p12 chr1: 999,355-1,042,016	AGRN, HES4, 2 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
nsv6628441	copy number variation	1	nstd224	human		GRCh37 chr3: 113,881,623-114,026,974 , GRCh38.p12 chr3: 114,162,776-114,308,127	TIGIT, DRD3, 2 more genes
nsv6625363	copy number variation	2	nstd224	human		GRCh37 chr1: 12,885,336-12,921,311 , GRCh38.p12 chr1: 12,825,478-12,861,456 , GRCh38.p12 chr1\|NW_012132914.1: 6,991-42,969	PRAMEF2, PRAMEF11, 2 more genes
nsv6629754	copy number variation	17	nstd224	human		GRCh37 chr4: 9,371,116-9,496,079 , GRCh38.p12 chr4: 9,369,390-9,494,435	OR7E85P, OR7E84P, 8 more genes

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