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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3117647copy number variation1estd209human GRCh37 chr8: 96,162,655-96,162,656 , GRCh38.p12 chr8: 95,150,427-95,150,428 PLEKHF2
    esv3117645copy number variation1estd209human GRCh37 chr8: 96,150,641-96,150,642 , GRCh38.p12 chr8: 95,138,413-95,138,414 PLEKHF2
    esv3371147copy number variation8estd59human NCBI36 chr8: 96,214,377-96,216,925 , GRCh37.p13 chr8: 96,145,201-96,147,749 , GRCh38.p12 chr8: 95,132,973-95,135,521 PLEKHF2
    esv3428037copy number variation1estd59human NCBI36 chr8: 96,218,091-96,218,319 , GRCh37.p13 chr8: 96,148,915-96,149,143 , GRCh38.p12 chr8: 95,136,687-95,136,915 PLEKHF2
    nsv819397copy number variation1nstd43human NCBI36 chr8: 96,237,431-96,246,854 , GRCh37.p13 chr8: 96,168,255-96,177,678 , GRCh38.p12 chr8: 95,156,027-95,165,450 PLEKHF2
    esv2471392copy number variation1estd197human NCBI36 chr8: 96,223,125-96,223,125 , GRCh37.p13 chr8: 96,153,949-96,153,949 , GRCh38.p12 chr8: 95,141,721-95,141,721 PLEKHF2
    esv2461041copy number variation1estd197human NCBI36 chr8: 96,231,832-96,231,832 , GRCh37.p13 chr8: 96,162,656-96,162,656 , GRCh38.p12 chr8: 95,150,428-95,150,428 PLEKHF2
    esv2302704copy number variation1estd194human NCBI36 chr8: 96,231,832-96,231,833 , GRCh37.p13 chr8: 96,162,656-96,162,657 , GRCh38.p12 chr8: 95,150,428-95,150,429 PLEKHF2
    esv1352617copy number variation1estd22human NCBI36 chr8: 96,217,735-96,217,739 , GRCh37.p13 chr8: 96,148,559-96,148,563 , GRCh38.p12 chr8: 95,136,331-95,136,335 PLEKHF2
    esv1671363copy number variation1estd22human NCBI36 chr8: 96,231,834-96,231,835 , GRCh37.p13 chr8: 96,162,658-96,162,659 , GRCh38.p12 chr8: 95,150,430-95,150,431 PLEKHF2
    esv1596004copy number variation1estd22human NCBI36 chr8: 96,219,817-96,219,818 , GRCh37.p13 chr8: 96,150,641-96,150,642 , GRCh38.p12 chr8: 95,138,413-95,138,414 PLEKHF2
    nsv393744copy number variation1nstd6human NCBI35 chr8: 96,219,154-96,219,158 , GRCh37.p13 chr8: 96,149,978-96,149,982 , GRCh38.p12 chr8: 95,137,750-95,137,754 PLEKHF2
    nsv386061copy number variation1nstd6human NCBI35 chr8: 96,217,749-96,217,750 , GRCh37.p13 chr8: 96,148,573-96,148,574 , GRCh38.p12 chr8: 95,136,345-95,136,346 PLEKHF2
    nsv373440copy number variation1nstd6human NCBI35 chr8: 96,229,598-96,229,599 , GRCh37.p13 chr8: 96,160,422-96,160,423 , GRCh38.p12 chr8: 95,148,194-95,148,195 PLEKHF2
    nsv394524copy number variation1nstd6human NCBI35 chr8: 96,227,925-96,227,925 , GRCh37.p13 chr8: 96,158,749-96,158,749 , GRCh38.p12 chr8: 95,146,521-95,146,521 PLEKHF2
    nsv951459copy number variation1nstd73human GRCh37 chr8: 96,155,401-96,169,600 , GRCh38.p12 chr8: 95,143,173-95,157,372 PLEKHF2
    esv3784061tandem duplication1estd192human GRCh37 chr8: 96,143,468-96,152,974 , GRCh38.p12 chr8: 95,131,240-95,140,746 PLEKHF2
    esv2856915insertion1estd209human GRCh37 chr8: 96,153,017-96,153,017 , GRCh38.p12 chr8: 95,140,789-95,140,789 PLEKHF2
    esv2856913insertion1estd209human GRCh37 chr8: 96,152,037-96,152,037 , GRCh38.p12 chr8: 95,139,809-95,139,809 PLEKHF2
    esv2272827insertion1estd194human NCBI36 chr8: 96,232,963-96,232,963 , GRCh37.p13 chr8: 96,163,787-96,163,787 , GRCh38.p12 chr8: 95,151,559-95,151,559 PLEKHF2
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