OAT_71 AND nstd53 - dbVar - NCBI

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Items: 13

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv870441	copy number variation	1	nstd53	human		GRCh38.p12 chr9: 12,074,235-12,180,870 , NCBI36 chr9: 12,064,235-12,170,870 , GRCh37.p13 chr9: 12,074,235-12,180,870	LOC105375976
nsv870186	copy number variation	10	nstd53	human		NCBI36 chr1: 167,493,827-167,520,743 , GRCh38.p12 chr1: 169,257,965-169,284,881 , GRCh37.p13 chr1: 169,227,203-169,254,119	NME7
nsv869911	copy number variation	1	nstd53	human		GRCh38.p12 chr21: 14,812,324-14,838,258 , NCBI36 chr21: 15,106,516-15,132,450 , GRCh37.p13 chr21: 16,184,645-16,210,579	RBMX2P1, ASMER1
nsv869814	copy number variation	1	nstd53	human		NCBI36 chr1: 6,115,408-6,141,064 , GRCh38.p12 chr1: 6,132,761-6,158,417 , GRCh37.p13 chr1: 6,192,821-6,218,477	CHD5,
nsv869730	copy number variation	122	nstd53	human		GRCh38.p12 chr8: 39,377,532-39,528,580 , NCBI36 chr8: 39,354,208-39,505,256 , GRCh37.p13 chr8: 39,235,051-39,386,099	ADAM3A, ADAM5
nsv869689	copy number variation	1	nstd53	human		GRCh37.p13 chr3: 11,925,827-12,041,877 , GRCh38.p12 chr3: 11,884,353-12,000,403 , NCBI36 chr3: 11,900,827-12,016,877 , GRCh37.p13 chr3\|NW_003871060.1: 1-102,145 , GRCh38.p12 chr3\|NW_003871060.2: 1-102,145	NUP210P2, MARK2P20, 3 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
nsv869910	copy number variation	14	nstd53	human		GRCh38.p12 chr2: 241,914,496-242,092,126 , NCBI36 chr2: 242,505,320-242,682,950 , GRCh37.p13 chr2: 242,856,647-243,034,277 , GRCh38.p12 chr2\|NT_187647.1: 1-135,836 , GRCh38.p12 chr2\|NT_187523.1: 1-136,196	LOC285097, LINC01881, 4 more genes
nsv869577	copy number variation	64	nstd53	human		NCBI36 chr15: 18,867,344-19,943,194 , GRCh38.p12 chr15: 20,402,077-22,153,879 , GRCh37.p13 chr15: 20,607,330-22,441,830	NBEAP1, OR4H6P, 78 more genes
nsv870021	copy number variation	1	nstd53	human		NCBI36 chr12: 11,066,487-11,143,592 , GRCh38.p12 chr12: 11,022,621-11,099,726 , GRCh37.p13 chr12: 11,175,220-11,252,325 , GRCh38.p12 chr12\|NW_003571050.1: 221,327-330,679 , GRCh38.p12 chr12\|NT_187658.1: 221,315-295,041	PRH1, TAS2R43, 9 more genes
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
nsv870034	copy number variation	4	nstd53	human		GRCh38.p12 chr10: 45,662,767-47,923,579 , NCBI36 chr10: 45,478,221-47,172,534 , GRCh37.p13 chr10: 46,158,215-47,702,528 , GRCh37.p13 chr10\|NW_003871068.1: 1-2,010,264	CTSLP2, GDF2, 72 more genes
nsv870440	copy number variation	38	nstd53	human		GRCh38.p12 chr8: 7,382,028-7,896,002 , NCBI36 chr8: 7,226,960-7,790,934 , GRCh37.p13 chr8: 7,239,550-7,753,524	DEFB4A, HSPD1P3, 41 more genes

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