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Items: 1 to 20 of 419

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973261inversion1nstd209human GRCh38 chr2: 10,298,894-10,304,511 , GRCh37.p13 chr2: 10,439,020-10,444,637 HPCAL1, LOC101929691
    nsv5885147copy number variation1nstd209human GRCh38 chr2: 10,319,575-10,320,634 , GRCh37.p13 chr2: 10,459,701-10,460,760 HPCAL1
    nsv5871235copy number variation1nstd209human GRCh38 chr2: 10,331,920-10,331,981 , GRCh37.p13 chr2: 10,472,046-10,472,107 HPCAL1
    nsv5624119insertion1nstd207human GRCh38 chr2: 10,399,445-10,399,445 , GRCh37.p13 chr2: 10,539,571-10,539,571 HPCAL1
    nsv5622519insertion1nstd207human GRCh38 chr2: 10,399,405-10,399,405 , GRCh37.p13 chr2: 10,539,531-10,539,531 HPCAL1
    nsv5618488insertion1nstd207human GRCh38 chr2: 10,399,271-10,399,271 , GRCh37.p13 chr2: 10,539,397-10,539,397 HPCAL1
    nsv5617905insertion1nstd207human GRCh38 chr2: 10,399,588-10,399,588 , GRCh37.p13 chr2: 10,539,714-10,539,714 HPCAL1
    nsv5617444insertion1nstd207human GRCh38 chr2: 10,399,478-10,399,478 , GRCh37.p13 chr2: 10,539,604-10,539,604 HPCAL1
    nsv5616470insertion1nstd207human GRCh38 chr2: 10,399,229-10,399,229 , GRCh37.p13 chr2: 10,539,355-10,539,355 HPCAL1
    nsv5615829insertion1nstd207human GRCh38 chr2: 10,399,262-10,399,262 , GRCh37.p13 chr2: 10,539,388-10,539,388 HPCAL1
    nsv5613194insertion1nstd207human GRCh38 chr2: 10,399,220-10,399,220 , GRCh37.p13 chr2: 10,539,346-10,539,346 HPCAL1
    nsv5580737copy number variation1nstd207human GRCh38 chr2: 10,376,901-10,376,962 , GRCh37.p13 chr2: 10,517,027-10,517,088 HPCAL1
    nsv5567656copy number variation1nstd207human GRCh38 chr2: 10,331,920-10,331,981 , GRCh37.p13 chr2: 10,472,046-10,472,107 HPCAL1
    nsv5453223copy number variation1nstd206human GRCh38 chr2: 10,409,782-10,409,904 , GRCh37.p13 chr2: 10,549,908-10,550,030 HPCAL1
    nsv5452214copy number variation1nstd206human GRCh38 chr2: 10,411,790-10,417,705 , GRCh37.p13 chr2: 10,551,916-10,557,831 HPCAL1
    nsv5448857copy number variation1nstd206human GRCh38 chr2: 10,397,657-10,404,957 , GRCh37.p13 chr2: 10,537,783-10,545,083 HPCAL1
    nsv5438298copy number variation1nstd206human GRCh38 chr2: 10,302,562-10,302,680 , GRCh37.p13 chr2: 10,442,688-10,442,806 HPCAL1
    nsv5357842translocation1nstd200human GRCh38 chr2: 10,409,782-10,409,782 , GRCh38 chr2: 10,409,904-10,409,904 , GRCh37.p13 chr2: 10,549,908-10,549,908 , GRCh37.p13 chr2: 10,550,030-10,550,030 HPCAL1
    nsv5357834translocation1nstd200human GRCh38 chr2: 10,368,439-10,368,439 , GRCh38 chr2: 10,368,665-10,368,665 , GRCh37.p13 chr2: 10,508,565-10,508,565 , GRCh37.p13 chr2: 10,508,791-10,508,791 HPCAL1
    nsv5291714copy number variation1nstd204human GRCh38.p13 chr2: 10,415,193-10,415,669 , GRCh37.p13 chr2: 10,555,319-10,555,795 HPCAL1
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