CONTROL_35 AND nstd53 - 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
nsv870073	copy number variation	19	nstd53	human		GRCh38.p12 chr6: 303,298-347,329 , NCBI36 chr6: 248,298-292,329 , GRCh37.p13 chr6: 303,298-347,329	DUSP22
nsv870173	copy number variation	4	nstd53	human		NCBI36 chr18: 1,903,602-1,975,578 , GRCh37.p13 chr18: 1,913,602-1,985,578 , GRCh38.p12 chr18: 1,913,601-1,985,577	AIDAP3, LOC105371958
nsv869807	copy number variation	87	nstd53	human		NCBI36 chr11: 55,118,273-55,200,744 , GRCh37.p13 chr11: 55,361,697-55,444,168 , GRCh38.p12 chr11: 55,594,221-55,676,692	OR4V1P, OR4P4, 3 more genes
nsv869574	copy number variation	8	nstd53	human		GRCh38.p12 chr10: 133,475,375-133,558,930 , NCBI36 chr10: 135,138,869-135,222,424 , GRCh37.p13 chr10: 135,288,879-135,372,434	CYP2E1, OR7M1P, 3 more genes
nsv869590	copy number variation	24	nstd53	human		NCBI36 chr15: 19,846,001-19,933,992 , GRCh38.p12 chr15: 22,056,686-22,144,677 , GRCh37.p13 chr15: 22,344,637-22,432,628	OR4H6P, OR4N4, 4 more genes
nsv869711	copy number variation	90	nstd53	human		NCBI36 chr4: 69,099,876-69,643,272 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr: NaN-NaN	0
nsv869819	copy number variation	4	nstd53	human		NCBI36 chr1: 12,788,835-13,101,056 , GRCh38.p12 chr1: 12,806,112-13,110,997 , GRCh37.p13 chr1: 12,866,248-13,178,469	PRAMEF2, HNRNPCL1, 15 more genes
nsv869782	copy number variation	92	nstd53	human		NCBI36 chr14: 19,273,348-19,478,367 , GRCh38.p12 chr14: 19,735,349-19,940,368 , GRCh37.p13 chr14: 20,203,508-20,408,527	OR4K6P, OR4K5, 10 more genes
nsv869808	copy number variation	12	nstd53	human		NCBI36 chr14: 106,219,843-106,256,498 , GRCh38.p12 chr14: 106,692,781-106,777,214 , GRCh37.p13 chr14: 107,148,798-107,185,453	IGH, IGHVIII-67-4, 9 more genes

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