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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5946943copy number variation1nstd209human GRCh38 chr12: 76,035,071-76,035,282 , GRCh37.p13 chr12: 76,428,851-76,429,062 NAP1L1
    nsv5853265copy number variation1nstd209human GRCh38 chr12: 76,072,265-76,074,664 , GRCh37.p13 chr12: 76,466,045-76,468,444 NAP1L1
    nsv5500934copy number variation1nstd206human GRCh38 chr12: 76,069,603-82,449,398 , GRCh37.p13 chr12: 76,463,383-82,843,177 , E2F7, 65 more genes
    nsv5127815mobile element insertion1nstd203human GRCh38 chr12: 76,068,440-76,068,454 , GRCh37.p13 chr12: 76,462,220-76,462,234 NAP1L1
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv5032581inversion1nstd200human GRCh38 chr12: 67,763,754-90,678,993 , GRCh37.p13 chr12: 68,157,534-91,072,770 , LOC105369886, 255 more genes
    nsv5006126copy number variation1nstd200human GRCh38 chr12: 76,068,728-76,068,802 , GRCh37.p13 chr12: 76,462,508-76,462,582 NAP1L1
    nsv5006125copy number variation1nstd200human GRCh38 chr12: 76,068,537-76,068,616 , GRCh37.p13 chr12: 76,462,317-76,462,396 NAP1L1
    nsv5006124copy number variation1nstd200human GRCh38 chr12: 76,051,563-76,051,703 , GRCh37.p13 chr12: 76,445,343-76,445,483 NAP1L1
    nsv5006123copy number variation1nstd200human GRCh38 chr12: 76,037,813-76,040,511 , GRCh37.p13 chr12: 76,431,593-76,434,291 NAP1L1
    nsv4888823inversion1nstd200human GRCh37 chr12: 68,157,543-91,072,771 , GRCh38.p12 chr12: 67,763,763-90,678,994 , BEST3, 255 more genes
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4846846copy number variation1nstd200human GRCh37 chr12: 76,445,343-76,445,483 , GRCh38.p12 chr12: 76,051,563-76,051,703 NAP1L1
    nsv4844164copy number variation1nstd200human GRCh37 chr12: 76,462,508-76,462,582 , GRCh38.p12 chr12: 76,068,728-76,068,802 NAP1L1
    nsv4835407copy number variation1nstd200human GRCh37 chr12: 76,431,593-76,434,291 , GRCh38.p12 chr12: 76,037,813-76,040,511 NAP1L1
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 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
    nsv4572353mobile element insertion1nstd166human GRCh37.p13 chr12: 76,468,592-76,468,592 , GRCh38.p12 chr12: 76,074,812-76,074,812 NAP1L1
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