OSC5998 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
nsv6629898	copy number variation	832	nstd224	human		GRCh37 chr4: 69,401,172-69,435,811 , GRCh38.p12 chr4: 68,535,454-68,570,093	UGT2B17
nsv6631779	copy number variation	63	nstd224	human		GRCh37 chr7: 141,772,099-141,794,376 , GRCh38.p12 chr7: 142,072,299-142,094,576 , GRCh38.p12 chr7\|NT_187562.1: 34,179-56,456	MGAM
nsv6628887	copy number variation	15	nstd224	human		GRCh37 chr3: 8,825,741-8,859,490 , GRCh38.p12 chr3: 8,784,055-8,817,804	LOC107986061
nsv6623865	copy number variation	1	nstd224	human		GRCh37 chr16: 55,842,641-55,856,356 , GRCh38.p12 chr16: 55,808,729-55,822,444	CES1
nsv6633571	copy number variation	4	nstd224	human		GRCh37 chrX: 115,942,800-116,045,594 , GRCh38.p12 chrX: 116,808,832-116,911,626	LOC100126447, RNU6-1323P
nsv6621608	copy number variation	26	nstd224	human		GRCh37 chr12: 32,004,170-32,061,168 , GRCh38.p12 chr12: 31,851,236-31,908,234	LINC02422, RPLP2P4
nsv6629306	copy number variation	49	nstd224	human		GRCh37 chr3: 75,447,252-75,563,370 , GRCh38.p12 chr3: 75,398,101-75,514,219	LINC02018, FAM86DP, 2 more genes
nsv6626439	copy number variation	12	nstd224	human		GRCh37 chr1: 25,599,085-25,655,563 , GRCh38.p12 chr1: 25,272,594-25,329,072	RHD, SDHDP6, 2 more genes
nsv6628225	copy number variation	1	nstd224	human		GRCh37 chr2: 86,307,624-86,512,480 , GRCh38.p12 chr2: 86,080,501-86,285,357	IMMT, POLR1A, 5 more genes
nsv6631973	copy number variation	4	nstd224	human		GRCh37 chr7: 57,481,104-57,621,951 , GRCh38.p12 chr7: 57,421,392-57,562,245	ZNF716, SAPCD2P2, 4 more genes
nsv6622002	copy number variation	111	nstd224	human		GRCh37 chr14: 20,198,662-20,417,653 , GRCh38.p12 chr14: 19,730,503-19,949,494	OR4N1P, OR4K3, 11 more genes

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