OAT_14 AND nstd53 - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv869732	copy number variation	3	nstd53	human		GRCh38.p12 chr8: 16,080,633-16,167,727 , NCBI36 chr8: 15,982,513-16,069,607 , GRCh37.p13 chr8: 15,938,142-16,025,236	MSR1
nsv870310	copy number variation	1	nstd53	human		NCBI36 chr14: 54,026,402-54,080,184 , GRCh38.p12 chr14: 54,489,934-54,543,716 , GRCh37.p13 chr14: 54,956,652-55,010,434	CGRRF1
nsv869928	copy number variation	2	nstd53	human		GRCh38.p12 chr4: 8,193,342-8,213,121 , GRCh37.p13 chr4: 8,195,069-8,214,848 , NCBI36 chr4: 8,245,969-8,265,748	SH3TC1
nsv869636	copy number variation	3	nstd53	human		NCBI36 chr12: 55,876,439-55,899,981 , GRCh38.p12 chr12: 57,196,389-57,219,931 , GRCh37.p13 chr12: 57,590,172-57,613,714	LRP1, NXPH4
nsv869953	copy number variation	1	nstd53	human		NCBI36 chrX: 31,660,535-32,106,905 , GRCh37.p13 chrX: 31,750,614-32,196,984 , GRCh38.p12 chrX: 31,732,497-32,178,867	DMD, RNA5SP501
nsv869963	copy number variation	2	nstd53	human		NCBI36 chr16: 66,942,907-66,972,404 , GRCh38.p12 chr16: 68,351,503-68,381,000 , GRCh37.p13 chr16: 68,385,406-68,414,903	PRMT7, SMPD3
nsv869931	copy number variation	2	nstd53	human		NCBI36 chr1: 195,048,267-195,158,448 , GRCh38.p12 chr1: 196,812,514-196,922,695 , GRCh37.p13 chr1: 196,781,644-196,891,825	CFHR1, CFHR4, 2 more genes
nsv870217	copy number variation	24	nstd53	human		NCBI36 chr11: 55,118,273-55,187,282 , GRCh37.p13 chr11: 55,361,697-55,430,706 , GRCh38.p12 chr11: 55,594,221-55,663,230	OR4P4, OR4C11, 2 more genes
nsv870265	copy number variation	100	nstd53	human		NCBI36 chr22: 22,696,215-22,725,305 , GRCh37.p13 chr22: 24,366,215-24,395,305 , GRCh38.p12 chr22\|NT_187633.1: 260,390-289,480	GSTT1, LOC391322, 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
nsv869914	copy number variation	2	nstd53	human		GRCh38.p12 chr10: 46,157,935-47,923,579 , NCBI36 chr10: 46,399,331-47,021,415 , GRCh37.p13 chr10: 47,006,954-47,531,169 , GRCh37.p13 chr10\|NW_003871068.1: 431,049-2,010,264	CTSLP2, GDF2, 54 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
nsv870413	copy number variation	41	nstd53	human		GRCh38.p12 chr2: 34,472,710-34,513,110 , NCBI36 chr2: 34,551,281-34,591,681 , GRCh37.p13 chr2: 34,697,777-34,738,177	0
nsv870072	copy number variation	1	nstd53	human		GRCh37.p13 chr3: 162,483,397-162,630,179 , GRCh38.p12 chr3: 162,765,609-162,912,391 , NCBI36 chr3: 163,966,091-164,112,873	0

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