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Items: 1 to 20 of 203

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979733insertion1nstd209human GRCh38 chr15: 80,204,170-80,204,170 , GRCh37.p13 chr15: 80,496,512-80,496,512 CTXND1
    nsv5940931copy number variation1nstd209human GRCh38 chr15: 80,228,699-80,234,546 , GRCh37.p13 chr15: 80,521,041-80,526,888 CTXND1
    nsv5937695copy number variation1nstd209human GRCh38 chr15: 80,208,957-80,217,217 , GRCh37.p13 chr15: 80,501,299-80,509,559 CTXND1
    nsv5935349copy number variation1nstd209human GRCh38 chr15: 77,970,674-82,312,707 , GRCh37.p13 chr15: 78,263,016-82,605,043 , ST20, 91 more genes
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5864756copy number variation2nstd209human GRCh38 chr15: 80,209,043-80,210,442 , GRCh37.p13 chr15: 80,501,385-80,502,784 CTXND1
    nsv5864561copy number variation1nstd209human GRCh38 chr15: 80,211,743-80,212,892 , GRCh37.p13 chr15: 80,504,085-80,505,234 CTXND1
    nsv5858251copy number variation1nstd209human GRCh38 chr15: 80,207,743-80,215,385 , GRCh37.p13 chr15: 80,500,085-80,507,727 CTXND1
    nsv5847727copy number variation1nstd209human GRCh38 chr15: 80,228,900-80,234,432 , GRCh37.p13 chr15: 80,521,242-80,526,774 CTXND1
    nsv5530067copy number variation1nstd206human GRCh38 chr15: 80,228,711-80,234,509 , GRCh37.p13 chr15: 80,521,053-80,526,851 CTXND1
    nsv5517108copy number variation1nstd206human GRCh38 chr15: 80,206,571-80,206,695 , GRCh37.p13 chr15: 80,498,913-80,499,037 CTXND1
    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
    nsv5365380translocation1nstd200human GRCh38 chr20: 2,826,769-2,826,769 , GRCh38 chr15: 80,252,422-80,252,422 , GRCh37.p13 chr20: 2,807,415-2,807,415 , GRCh37.p13 chr15: 80,544,764-80,544,764 CTXND1
    nsv5142319mobile element insertion1nstd203human GRCh38 chr15: 80,204,146-80,204,170 , GRCh37.p13 chr15: 80,496,488-80,496,512 CTXND1
    nsv5059965copy number variation1nstd102humanUncertain significance GRCh38 chr15: 80,234,872-80,234,873 , GRCh37 chr15: 80,527,214-80,527,215 CTXND1
    nsv5009092copy number variation1nstd200human GRCh38 chr15: 80,237,434-80,256,444 , GRCh37.p13 chr15: 80,529,776-80,548,786 CTXND1
    nsv5001952copy number variation1nstd200human GRCh38 chr15: 80,228,351-80,230,032 , GRCh37.p13 chr15: 80,520,693-80,522,374 CTXND1
    nsv5001951copy number variation1nstd200human GRCh38 chr15: 80,220,725-80,221,010 , GRCh37.p13 chr15: 80,513,067-80,513,352 CTXND1
    nsv5001950copy number variation1nstd200human GRCh38 chr15: 80,208,511-80,209,727 , GRCh37.p13 chr15: 80,500,853-80,502,069 CTXND1
    nsv4992298copy number variation1nstd200human GRCh38 chr15: 73,152,590-82,101,178 , GRCh37.p13 chr15: 73,444,931-82,393,519 , SNUPN, 215 more genes
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