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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6921754copy number variation1nstd229human GRCh38 chr12: 52,392,147-52,392,721 , GRCh37.p13 chr12: 52,785,931-52,786,505 KRT82
    nsv4200534copy number variation1nstd166human GRCh37.p13 chr12: 52,795,027-52,795,333 , GRCh38.p12 chr12: 52,401,243-52,401,549 KRT82
    esv3162828copy number variation1estd209human GRCh37 chr12: 52,785,889-52,785,891 , GRCh38.p12 chr12: 52,392,105-52,392,107 KRT82
    esv3162829copy number variation1estd209human GRCh37 chr12: 52,789,693-52,789,694 , GRCh38.p12 chr12: 52,395,909-52,395,910 KRT82
    esv1027621copy number variation1estd22human NCBI36 chr12: 51,072,160-51,072,162 , GRCh37.p13 chr12: 52,785,893-52,785,895 , GRCh38.p12 chr12: 52,392,109-52,392,111 KRT82
    esv1395815copy number variation1estd22human NCBI36 chr12: 51,075,960-51,075,961 , GRCh37.p13 chr12: 52,789,693-52,789,694 , GRCh38.p12 chr12: 52,395,909-52,395,910 KRT82
    nsv51971copy number variation1nstd6human NCBI35 chr12: 51,075,961-51,075,961 , GRCh37.p13 chr12: 52,789,694-52,789,694 , GRCh38.p12 chr12: 52,395,910-52,395,910 KRT82
    nsv6924141copy number variation1nstd229human GRCh38 chr12: 52,395,885-52,396,239 , GRCh37.p13 chr12: 52,789,669-52,790,023 KRT82
    nsv3147756copy number variation1nstd151human GRCh37 chr12: 52,793,766-52,800,066 , GRCh38.p12 chr12: 52,399,982-52,406,282 KRT82
    esv1361238insertion1estd22human NCBI36 chr12: 51,072,280-51,072,280 , GRCh37.p13 chr12: 52,786,013-52,786,013 , GRCh38.p12 chr12: 52,392,229-52,392,229 KRT82
    nsv1640731short tandem repeat1nstd128human GRCh37 chr12: 52,791,840-52,791,861 , GRCh38.p12 chr12: 52,398,056-52,398,077 KRT82
    nsv1681402short tandem repeat4nstd128human GRCh37 chr12: 52,792,266-52,792,281 , GRCh38.p12 chr12: 52,398,482-52,398,497 KRT82
    nsv1681403short tandem repeat2nstd128human GRCh37 chr12: 52,797,241-52,797,253 , GRCh38.p12 chr12: 52,403,457-52,403,469 KRT82
    nsv6921453copy number variation1nstd229human GRCh38 chr12: 52,379,131-52,395,078 , GRCh37.p13 chr12: 52,772,915-52,788,862 KRT84, KRT82
    nsv6929196copy number variation1nstd229human GRCh38 chr12: 52,404,670-52,417,095 , GRCh37.p13 chr12: 52,798,454-52,810,879 KRT90P, KRT82
    nsv3150103copy number variation1nstd151human GRCh37 chr12: 52,773,657-52,789,579 , GRCh38.p12 chr12: 52,379,873-52,395,795 KRT84, KRT82
    esv3802466tandem duplication1estd192human GRCh37 chr12: 52,798,442-52,814,732 , GRCh38.p12 chr12: 52,404,658-52,420,948 KRT90P, KRT82
    nsv3232466insertion4nstd152human GRCh38 chr12: 52,404,214-52,419,803 , GRCh37.p13 chr12: 52,797,998-52,813,587 KRT90P, KRT82
    nsv3150842copy number variation1nstd151human GRCh37 chr12: 52,774,861-52,828,093 , GRCh38.p12 chr12: 52,381,077-52,434,309 KRT82, KRT90P, 2 more genes
    nsv558928copy number variation1nstd54human NCBI36 chr12: 51,081,854-51,117,336 , GRCh37.p13 chr12: 52,795,587-52,831,069 , GRCh38.p12 chr12: 52,401,803-52,437,285 KRT82, KRT90P, 1 more genes
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