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Items: 1 to 20 of 215

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978550insertion1nstd209human GRCh38 chr12: 110,318,845-110,318,845 , GRCh37.p13 chr12: 110,756,650-110,756,650 ATP2A2
    nsv5702537mobile element insertion1nstd211human GRCh38 chr12: 110,283,794-110,283,794 , GRCh37.p13 chr12: 110,721,599-110,721,599 ATP2A2
    nsv5672791copy number variation1nstd102humanPathogenic GRCh37 chr12: 110,719,595-110,720,600 , GRCh38.p12 chr12: 110,281,790-110,282,795 ATP2A2
    nsv5497506copy number variation1nstd206human GRCh38 chr12: 110,294,303-110,294,692 , GRCh37.p13 chr12: 110,732,108-110,732,497 ATP2A2
    nsv5496837copy number variation1nstd206human GRCh38 chr12: 110,300,041-110,300,169 , GRCh37.p13 chr12: 110,737,846-110,737,974 ATP2A2
    nsv5420149mobile element insertion1nstd206human GRCh38 chr12: 110,283,794-110,283,845 , GRCh37.p13 chr12: 110,721,599-110,721,650 ATP2A2
    nsv5363975translocation1nstd200human GRCh38 chr8: 30,285,203-30,285,203 , GRCh38 chr12: 110,314,060-110,314,060 , GRCh37.p13 chr12: 110,751,865-110,751,865 , GRCh37.p13 chr8: 30,142,719-30,142,719 ATP2A2
    nsv5128451mobile element insertion1nstd203human GRCh38 chr12: 110,283,785-110,283,794 , GRCh37.p13 chr12: 110,721,590-110,721,599 ATP2A2
    nsv4995570copy number variation1nstd200human GRCh38 chr12: 110,319,704-110,319,756 , GRCh37.p13 chr12: 110,757,509-110,757,561 ATP2A2
    nsv4995569copy number variation1nstd200human GRCh38 chr12: 110,303,619-110,305,090 , GRCh37.p13 chr12: 110,741,424-110,742,895 ATP2A2
    nsv4993671copy number variation1nstd200human GRCh38 chr12: 110,217,708-110,299,994 , GRCh37.p13 chr12: 110,655,513-110,737,799 IFT81, ATP2A2
    nsv4842226copy number variation1nstd200human GRCh37 chr12: 110,757,509-110,757,561 , GRCh38.p12 chr12: 110,319,704-110,319,756 ATP2A2
    nsv4835770copy number variation1nstd200human GRCh37 chr12: 110,655,513-110,737,799 , GRCh38.p12 chr12: 110,217,708-110,299,994 IFT81, ATP2A2
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4754840inversion1nstd199human GRCh37 chr12: 104,382,539-125,801,164 , GRCh38.p12 chr12: 103,988,761-125,316,618 , ACACB, 452 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4728881copy number variation1nstd102humanPathogenic GRCh37 chr12: 106,498,814-112,252,906 , GRCh38.p12 chr12: 106,105,036-111,815,102 ATP2A2, CUX2, 115 more genes
    nsv4608409copy number variation1nstd183human GRCh37 chr12: 110,718,803-110,719,498 , GRCh38.p12 chr12: 110,280,998-110,281,693 ATP2A2
    nsv4560276mobile element insertion1nstd166human GRCh37.p13 chr12: 110,759,766-110,759,766 , GRCh38.p12 chr12: 110,321,961-110,321,961 ATP2A2
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