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Items: 1 to 20 of 258

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146427copy number variation1nstd232human GRCh37.p13 chr6: 134,796,948-134,797,067 , GRCh38.p12 chr6: 134,475,810-134,475,929 LINC01010, CT69
    nsv7144801insertion1nstd232human GRCh37.p13 chr6: 134,770,501-134,770,501 , GRCh38.p12 chr6: 134,449,363-134,449,363 LINC01010, CT69
    nsv7042243inversion1nstd229human GRCh38 chr6: 134,467,494-134,468,085 , GRCh37.p13 chr6: 134,788,632-134,789,223 CT69, LINC01010
    nsv7040961inversion1nstd229human GRCh38 chr6: 131,090,546-134,695,837 , GRCh37.p13 chr6: 131,411,686-135,016,975 ENPP3, MOXD1, 70 more genes
    nsv6816182copy number variation1nstd229human GRCh38 chr6: 134,430,001-134,433,700 , GRCh37.p13 chr6: 134,751,139-134,754,838 CT69
    nsv6811263copy number variation1nstd229human GRCh38 chr6: 134,452,227-134,461,015 , GRCh37.p13 chr6: 134,773,365-134,782,153 LINC01010, CT69
    nsv6808730copy number variation1nstd229human GRCh38 chr6: 134,415,240-134,428,242 , GRCh37.p13 chr6: 134,736,378-134,749,380 CT69
    nsv6807331copy number variation1nstd229human GRCh38 chr6: 134,409,841-135,998,734 , GRCh37.p13 chr6: 134,730,979-136,319,872 MYB, LINC01010, 21 more genes
    nsv6806507copy number variation1nstd229human GRCh38 chr6: 134,445,074-134,445,495 , GRCh37.p13 chr6: 134,766,212-134,766,633 CT69, LINC01010
    nsv6803755copy number variation1nstd229human GRCh38 chr6: 134,460,520-134,823,328 , GRCh37.p13 chr6: 134,781,658-135,144,466 FAM8A6P, LINC03002, 3 more genes
    nsv6803044copy number variation1nstd229human GRCh38 chr6: 134,460,636-134,464,367 , GRCh37.p13 chr6: 134,781,774-134,785,505 CT69, LINC01010
    nsv6802467copy number variation1nstd229human GRCh38 chr6: 134,472,640-134,472,751 , GRCh37.p13 chr6: 134,793,778-134,793,889 LINC01010, CT69
    nsv6799515copy number variation1nstd229human GRCh38 chr6: 134,445,500-134,449,632 , GRCh37.p13 chr6: 134,766,638-134,770,770 LINC01010, CT69
    nsv6564051inversion1nstd223human GRCh38 chr6: 134,440,239-134,441,358 , GRCh37.p13 chr6: 134,761,377-134,762,496 CT69, LINC01010
    nsv6559803inversion1nstd223human GRCh38 chr6: 134,471,313-134,471,503 , GRCh37.p13 chr6: 134,792,451-134,792,641 CT69, LINC01010
    nsv6558396inversion1nstd223human GRCh38 chr6: 134,463,060-134,463,417 , GRCh37.p13 chr6: 134,784,198-134,784,555 CT69, LINC01010
    nsv6558019inversion1nstd223human GRCh38 chr6: 134,462,784-134,463,569 , GRCh37.p13 chr6: 134,783,922-134,784,707 CT69, LINC01010
    nsv6290946copy number variation1nstd102humanPathogenic GRCh37 chr6: 130,769,034-136,009,217 , GRCh38.p12 chr6: 130,447,889-135,688,079 LOC105378004, LINC01010, 89 more genes
    nsv6269706copy number variation1nstd214human GRCh38 chr6: 134,475,900-134,475,961 , GRCh37.p13 chr6: 134,797,038-134,797,099 CT69, LINC01010
    nsv6266128copy number variation1nstd214human GRCh38 chr6: 134,475,791-134,475,850 , GRCh37.p13 chr6: 134,796,929-134,796,988 CT69, LINC01010
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