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Items: 1 to 20 of 184

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6115056mobile element insertion1nstd186human GRCh37 chr9: 91,947,691-91,947,691 , GRCh38.p12 chr9: 89,332,776-89,332,776 SECISBP2
    nsv5963474insertion1nstd209human GRCh38 chr9: 89,332,776-89,332,776 , GRCh37.p13 chr9: 91,947,691-91,947,691 SECISBP2
    nsv5699809mobile element insertion2nstd211human GRCh38 chr9: 89,332,792-89,332,792 , GRCh37.p13 chr9: 91,947,707-91,947,707 SECISBP2
    nsv5640508insertion1nstd207human GRCh38 chr9: 89,332,776-89,332,776 , GRCh37.p13 chr9: 91,947,691-91,947,691 SECISBP2
    nsv5626937insertion1nstd207human GRCh38 chr9: 89,317,696-89,317,696 , GRCh37.p13 chr9: 91,932,611-91,932,611 SECISBP2
    nsv5488709copy number variation1nstd206human GRCh38 chr9: 89,357,566-89,357,996 , GRCh37.p13 chr9: 91,972,481-91,972,911 SECISBP2
    nsv5488223copy number variation1nstd206human GRCh38 chr9: 89,349,929-89,350,631 , GRCh37.p13 chr9: 91,964,844-91,965,546 SECISBP2
    nsv5488068copy number variation1nstd206human GRCh38 chr9: 89,358,191-89,358,720 , GRCh37.p13 chr9: 91,973,106-91,973,635 SECISBP2
    nsv5486418copy number variation1nstd206human GRCh38 chr9: 89,326,038-89,328,656 , GRCh37.p13 chr9: 91,940,953-91,943,571 SECISBP2
    nsv5484292copy number variation1nstd206human GRCh38 chr9: 89,347,048-89,348,075 , GRCh37.p13 chr9: 91,961,963-91,962,990 SECISBP2
    nsv5479619copy number variation1nstd206human GRCh38 chr9: 89,360,452-89,361,675 , GRCh37.p13 chr9: 91,975,367-91,976,590 SECISBP2, SEMA4D
    nsv5479408copy number variation1nstd206human GRCh38 chr9: 89,348,215-89,349,773 , GRCh37.p13 chr9: 91,963,130-91,964,688 SECISBP2
    nsv5477898copy number variation1nstd206human GRCh38 chr9: 89,334,730-89,338,455 , GRCh37.p13 chr9: 91,949,645-91,953,370 SECISBP2
    nsv5401898mobile element insertion1nstd206human GRCh38 chr9: 89,332,776-89,332,776 , GRCh37.p13 chr9: 91,947,691-91,947,691 SECISBP2
    nsv5372767translocation1nstd200human GRCh38 chr9: 89,358,720-89,358,720 , GRCh38 chr9: 89,358,190-89,358,190 , GRCh37.p13 chr9: 91,973,635-91,973,635 , GRCh37.p13 chr9: 91,973,105-91,973,105 SECISBP2
    nsv5337050translocation1nstd200human GRCh37 chr9: 91,973,106-91,973,106 , GRCh37 chr9: 91,973,635-91,973,635 , GRCh38.p12 chr9: 89,358,191-89,358,191 , GRCh38.p12 chr9: 89,358,720-89,358,720 SECISBP2
    nsv5301358copy number variation1nstd204human GRCh37.p13 chr9: 91,975,342-91,976,611 , GRCh38.p13 chr9: 89,360,427-89,361,696 SEMA4D, SECISBP2
    nsv5252563copy number variation1nstd204human GRCh38.p13 chr9: 89,360,419-89,361,718 , GRCh37.p13 chr9: 91,975,334-91,976,633 SECISBP2, SEMA4D
    nsv5246440copy number variation1nstd204human GRCh38.p13 chr9: 89,308,401-89,318,600 , GRCh37.p13 chr9: 91,923,316-91,933,515 MIR3153, SECISBP2, 2 more genes
    nsv5138714mobile element insertion1nstd203human GRCh38 chr9: 89,336,081-89,336,108 , GRCh37.p13 chr9: 91,950,996-91,951,023 SECISBP2
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