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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5946436copy number variation1nstd209human GRCh38 chr15: 75,639,891-75,639,955 , GRCh37.p13 chr15: 75,932,232-75,932,296 IMP3
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5928357copy number variation1nstd209human GRCh38 chr15: 75,270,339-75,786,969 , GRCh37.p13 chr15: 75,562,680-76,079,310 LOC101929408, RN7SL319P, 23 more genes
    nsv5532304copy number variation1nstd206human GRCh38 chr15: 75,639,891-75,639,956 , GRCh37.p13 chr15: 75,932,232-75,932,297 IMP3
    nsv5380975copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,596,353-76,103,430 , GRCh38.p12 chr15: 75,304,012-75,811,089 RPL13P4, PTPN9, 20 more genes
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5274325copy number variation1nstd204human GRCh38.p13 chr15: 75,481,301-75,644,900 , GRCh37.p13 chr15: 75,773,642-75,937,241 LOC107984720, PTPN9, 3 more genes
    nsv5009065copy number variation1nstd200human GRCh38 chr15: 75,638,539-75,639,070 , GRCh37.p13 chr15: 75,930,880-75,931,411 IMP3
    nsv4992298copy number variation1nstd200human GRCh38 chr15: 73,152,590-82,101,178 , GRCh37.p13 chr15: 73,444,931-82,393,519 , SNUPN, 215 more genes
    nsv4729733copy number variation1nstd102humanUncertain significance GRCh37 chr15: 75,920,400-76,632,051 , GRCh38.p12 chr15: 75,628,059-76,339,710 ISL2, TYRO3P, 18 more genes
    nsv4729106copy number variation1nstd102humanPathogenic GRCh37 chr15: 74,398,162-76,054,094 , GRCh38.p12 chr15: 74,105,821-75,761,753 FAM219B, MIR4513, 62 more genes
    nsv4728988copy number variation1nstd102humanUncertain significance GRCh37 chr15: 75,440,382-76,133,553 , GRCh38.p12 chr15: 75,148,041-75,841,212 RPL13P4, PTPN9, 30 more genes
    nsv4457005copy number variation1nstd102humanUncertain significance GRCh37 chr15: 75,309,345-75,930,806 , GRCh38.p12 chr15: 75,017,004-75,638,465 LOC100128721, SNUPN, 23 more genes
    nsv4456751copy number variation1nstd102humanUncertain significance GRCh37 chr15: 75,508,057-76,128,091 , GRCh38.p12 chr15: 75,215,716-75,835,750 GOLGA6C, COMMD4, 27 more genes
    nsv4455912copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,963,271-76,064,900 , GRCh38.p12 chr15: 72,670,930-75,772,559 MIR6881, ARID3B, 94 more genes
    nsv4382078copy number variation1nstd173human GRCh37 chr15: 75,877,215-75,991,451 , GRCh38.p12 chr15: 75,584,874-75,699,110 SNUPN, CSPG4, 2 more genes
    nsv4370284copy number variation2nstd173human GRCh37 chr15: 75,877,357-75,974,622 , GRCh38.p12 chr15: 75,585,016-75,682,281 SNUPN, CSPG4, 2 more genes
    nsv4349273copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,648,132-76,102,251 , GRCh38.p12 chr15: 75,355,791-75,809,910 SNUPN, GOLGA6EP, 17 more genes
    nsv4252030copy number variation1nstd166human GRCh37.p13 chr15: 75,932,232-75,932,297 , GRCh38.p12 chr15: 75,639,891-75,639,956 IMP3
    nsv4247829copy number variation1nstd166human GRCh37.p13 chr15: 75,831,948-75,952,401 , GRCh38.p12 chr15: 75,539,607-75,660,060 SNUPN, SNX33, 2 more genes
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