OSC8306 AND nstd224 - dbVar - NCBI

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Items: 9

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Number of Variants: 9

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
nsv6624001	copy number variation	1	nstd224	human		GRCh37 chr16: 89,856,524-89,877,346 , GRCh38.p12 chr16: 89,790,116-89,810,938	FANCA
nsv6628033	copy number variation	112	nstd224	human		GRCh37 chr2: 242,867,913-243,007,368 , GRCh38.p12 chr2: 241,925,762-242,065,217 , GRCh38.p12 chr2\|NT_187523.1: 1-109,287 , GRCh38.p12 chr2\|NT_187647.1: 1-108,927	LINC01238, LINC01880, 3 more genes
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
nsv6626369	copy number variation	153	nstd224	human		GRCh37 chr1: 25,604,951-25,655,563 , GRCh38.p12 chr1: 25,278,460-25,329,072	RSRP1, RHD, 1 more genes
nsv6627077	copy number variation	11	nstd224	human		GRCh37 chr22: 24,301,973-24,386,612 , GRCh38.p12 chr22: 23,959,786-24,002,279 , GRCh38.p12 chr22\|NT_187633.1: 196,148-280,787	GSTT2, LOC391322, 10 more genes
nsv6622311	copy number variation	18	nstd224	human		GRCh37 chr14: 45,201,353-45,224,071 , GRCh38.p12 chr14: 44,732,150-44,754,868	0
nsv6625289	copy number variation	12	nstd224	human		GRCh37 chr19: 53,932,295-54,014,838 , GRCh38.p12 chr19: 53,429,042-53,511,584	ZNF331, ZNF813, 7 more genes
nsv6620628	copy number variation	93	nstd224	human		GRCh37 chr10: 47,146,867-47,703,869 , GRCh38.p12 chr10: 46,157,935-47,739,149	GDF10, RBP3, 48 more genes

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OSC8306 AND nstd224 (10)
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