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Items: 1 to 20 of 187

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129681insertion1nstd186human GRCh37 chr15: 78,424,618-78,424,618 , GRCh38.p12 chr15: 78,132,276-78,132,276 CIB2
    nsv5973767insertion1nstd209human GRCh38 chr15: 78,132,276-78,132,276 , GRCh37.p13 chr15: 78,424,618-78,424,618 CIB2
    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
    nsv5659446insertion1nstd207human GRCh38 chr15: 78,132,272-78,132,272 , GRCh37.p13 chr15: 78,424,614-78,424,614 CIB2
    nsv5564219copy number variation1nstd102humanUncertain significance GRCh37 chr15: 78,416,047-78,423,557 , GRCh38.p12 chr15: 78,123,705-78,131,215 CIB2
    nsv5556515sequence alteration1nstd206human GRCh38 chr15: 77,975,462-78,778,174 , GRCh37.p13 chr15: 78,267,804-79,070,516 , CHRNA5, 26 more genes
    nsv5544450insertion1nstd206human GRCh38 chr15: 78,132,276-78,132,276 , GRCh37.p13 chr15: 78,424,618-78,424,618 CIB2
    nsv5380979copy number variation1nstd102humanUncertain significance GRCh37 chr15: 78,423,487-78,423,557 , GRCh38.p12 chr15: 78,131,145-78,131,215 CIB2
    nsv5380844copy number variation1nstd102humanUncertain significance GRCh37 chr15: 78,397,653-78,423,557 , GRCh38.p12 chr15: 78,105,311-78,131,215 CIB2
    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
    nsv5380146translocation1nstd200human GRCh38 chr15: 78,138,883-78,138,883 , GRCh38 chr15: 78,130,432-78,130,432 , GRCh37.p13 chr15: 78,431,225-78,431,225 , GRCh37.p13 chr15: 78,422,774-78,422,774 CIB2
    nsv5303566copy number variation1nstd204human GRCh38.p13 chr15: 78,126,242-78,145,459 , GRCh37.p13 chr15: 78,418,584-78,437,801 CIB2
    nsv5274223copy number variation1nstd204human GRCh38.p13 chr15: 78,127,511-78,129,610 , GRCh37.p13 chr15: 78,419,853-78,421,952 CIB2
    nsv5265624copy number variation1nstd204human GRCh38.p13 chr15: 78,132,055-78,133,154 , GRCh37.p13 chr15: 78,424,397-78,425,496 CIB2
    nsv5261598copy number variation1nstd204human GRCh38.p13 chr15: 78,122,046-78,145,365 , GRCh37.p13 chr15: 78,414,388-78,437,707 CIB2
    nsv5159152mobile element insertion1nstd203human GRCh38 chr15: 78,132,265-78,132,276 , GRCh37.p13 chr15: 78,424,607-78,424,618 CIB2
    nsv5151598mobile element insertion1nstd203human GRCh38 chr15: 78,132,267-78,132,276 , GRCh37.p13 chr15: 78,424,609-78,424,618 CIB2
    nsv5148116mobile element insertion1nstd203human GRCh38 chr15: 78,132,280-78,132,325 , GRCh37.p13 chr15: 78,424,622-78,424,667 CIB2
    nsv5147862mobile element insertion1nstd203human GRCh38 chr15: 78,132,272-78,132,324 , GRCh37.p13 chr15: 78,424,614-78,424,666 CIB2
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