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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099226copy number variation1nstd231human GRCh38.p12 chr1: 115,063,638-119,984,872 , GRCh37 chr1: 115,606,259-120,527,495 ATP1A1, CASQ2, 103 more genes
    nsv7095241copy number variation1nstd102humanPathogenic GRCh37 chr1: 119,466,351-120,286,570 , GRCh38.p12 chr1: 118,923,728-119,743,947 HAO2-IT1, LINC01780, 29 more genes
    nsv6640996copy number variation1nstd229human GRCh38 chr1: 119,180,006-119,885,056 , GRCh37.p13 chr1: 119,722,629-120,427,679 PHGDH, NOTCH2P1, 28 more genes
    nsv6640880copy number variation1nstd229human GRCh38 chr1: 119,560,701-119,599,700 , GRCh37.p13 chr1: 120,103,324-120,142,323 HSD3BP4, GAPDHP33, 2 more genes
    nsv6640876copy number variation1nstd229human GRCh38 chr1: 119,294,157-119,747,268 , GRCh37.p13 chr1: 119,836,780-120,289,891 ZNF697, HSD3BP3, 21 more genes
    nsv6637125copy number variation1nstd102humanUncertain significance GRCh37 chr1: 119,836,835-120,151,604 , GRCh38.p12 chr1: 119,294,212-119,608,981 HSD3BP4, GAPDHP33, 17 more genes
    nsv6625595copy number variation1nstd224human GRCh37 chr1: 120,134,599-120,149,428 , GRCh38.p12 chr1: 119,591,976-119,606,805 HSD3BP5, LINC00622, 1 more genes
    nsv6625594copy number variation2nstd224human GRCh37 chr1: 120,133,331-120,154,662 , GRCh38.p12 chr1: 119,590,708-119,612,039 GAPDHP33, LINC00622, 1 more genes
    nsv6625593copy number variation1nstd224human GRCh37 chr1: 120,133,331-120,152,887 , GRCh38.p12 chr1: 119,590,708-119,610,264 LINC00622, GAPDHP33, 1 more genes
    nsv6625109copy number variation1nstd224human GRCh37 chr1: 120,133,331-120,148,707 , GRCh38.p12 chr1: 119,590,708-119,606,084 LINC00622, HSD3BP5, 1 more genes
    nsv6625108copy number variation3nstd224human GRCh37 chr1: 120,123,179-120,143,753 , GRCh38.p12 chr1: 119,580,556-119,601,130 GAPDHP33, LINC00622, 1 more genes
    nsv6625107copy number variation1nstd224human GRCh37 chr1: 120,110,175-120,138,931 , GRCh38.p12 chr1: 119,567,552-119,596,308 GAPDHP33, LINC00622, 1 more genes
    nsv6332826copy number variation1nstd223human GRCh38 chr1: 119,386,345-119,599,790 , GRCh37.p13 chr1: 119,928,968-120,142,413 HAO2, GAPDHP32, 14 more genes
    nsv6330137copy number variation1nstd223human GRCh38 chr1: 119,570,759-119,607,922 , GRCh37.p13 chr1: 120,113,382-120,150,545 HSD3BP4, HSD3BP5, 2 more genes
    nsv6325268copy number variation1nstd223human GRCh38 chr1: 119,582,022-119,613,006 , GRCh37.p13 chr1: 120,124,645-120,155,629 GAPDHP33, HSD3BP5, 1 more genes
    nsv6319150copy number variation1nstd223human GRCh38 chr1: 119,571,997-119,609,115 , GRCh37.p13 chr1: 120,114,620-120,151,738 HSD3BP5, LINC00622, 2 more genes
    nsv6317304copy number variation1nstd223human GRCh38 chr1: 119,587,671-119,618,580 , GRCh37.p13 chr1: 120,130,294-120,161,203 LINC00622, HSD3BP5, 2 more genes
    nsv6313671copy number variation1nstd102humanPathogenic GRCh37 chr1: 111,647,582-121,343,783 , GRCh38.p12 chr1: 111,104,960-121,601,985 GAPDHP23, RNA5SP56, 243 more genes
    nsv6310719copy number variation1nstd102humanUncertain significance GRCh37 chr1: 119,618,953-120,311,467 , GRCh38.p12 chr1: 119,076,330-119,768,844 LOC105378937, HMGCS2, 27 more genes
    nsv6310669copy number variation2nstd102humanUncertain significance GRCh37 chr1: 119,427,355-120,529,725 , GRCh38.p12 chr1: 118,884,732-119,987,102 NOTCH2P1, NOTCH2, 36 more genes
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