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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3914843insertion1nstd102humanBenign GRCh38 chr15: 66,443,587-66,443,588 , GRCh37.p13 chr15: 66,735,925-66,735,926 MAP2K1
    nsv4246478copy number variation1nstd166human GRCh37.p13 chr15: 66,683,749-66,684,580 , GRCh38.p12 chr15: 66,391,411-66,392,242 MAP2K1
    nsv4249329copy number variation1nstd166human GRCh37.p13 chr15: 66,755,118-66,755,204 , GRCh38.p12 chr15: 66,462,780-66,462,866 MAP2K1
    nsv4240817copy number variation1nstd166human GRCh37.p13 chr15: 66,761,831-66,761,887 , GRCh38.p12 chr15: 66,469,493-66,469,549 MAP2K1
    nsv3214476copy number variation2nstd152human GRCh38 chr15: 66,469,855-66,470,159 , GRCh37.p13 chr15: 66,762,193-66,762,497 MAP2K1
    nsv3213308copy number variation1nstd152human GRCh38 chr15: 66,469,680-66,469,810 , GRCh37.p13 chr15: 66,762,018-66,762,148 MAP2K1
    nsv1183775copy number variation226nstd112Neandertal, Denisova hominin, human GRCh37 chr15: 66,752,283-66,763,963 , GRCh38.p12 chr15: 66,459,945-66,471,625 MAP2K1
    esv3192388copy number variation1estd209human GRCh37 chr15: 66,722,003-66,722,018 , GRCh38.p12 chr15: 66,429,665-66,429,680 MAP2K1
    esv3192393copy number variation1estd209human GRCh37 chr15: 66,761,999-66,762,003 , GRCh38.p12 chr15: 66,469,661-66,469,665 MAP2K1
    esv3192383copy number variation1estd209human GRCh37 chr15: 66,712,122-66,712,126 , GRCh38.p12 chr15: 66,419,784-66,419,788 MAP2K1
    esv3192381copy number variation1estd209human GRCh37 chr15: 66,702,761-66,702,765 , GRCh38.p12 chr15: 66,410,423-66,410,427 MAP2K1
    esv3192387copy number variation1estd209human GRCh37 chr15: 66,721,688-66,721,690 , GRCh38.p12 chr15: 66,429,350-66,429,352 MAP2K1
    esv3192386copy number variation1estd209human GRCh37 chr15: 66,718,480-66,718,482 , GRCh38.p12 chr15: 66,426,142-66,426,144 MAP2K1
    esv3192376copy number variation1estd209human GRCh37 chr15: 66,683,395-66,683,397 , GRCh38.p12 chr15: 66,391,057-66,391,059 MAP2K1
    esv3192392copy number variation1estd209human GRCh37 chr15: 66,755,850-66,755,851 , GRCh38.p12 chr15: 66,463,512-66,463,513 MAP2K1
    esv3192390copy number variation1estd209human GRCh37 chr15: 66,751,647-66,751,648 , GRCh38.p12 chr15: 66,459,309-66,459,310 MAP2K1
    esv3192389copy number variation1estd209human GRCh37 chr15: 66,734,090-66,734,091 , GRCh38.p12 chr15: 66,441,752-66,441,753 MAP2K1
    esv3192385copy number variation1estd209human GRCh37 chr15: 66,717,721-66,717,722 , GRCh38.p12 chr15: 66,425,383-66,425,384 MAP2K1
    esv3192384copy number variation1estd209human GRCh37 chr15: 66,712,722-66,712,723 , GRCh38.p12 chr15: 66,420,384-66,420,385 MAP2K1
    esv3192382copy number variation1estd209human GRCh37 chr15: 66,711,858-66,711,859 , GRCh38.p12 chr15: 66,419,520-66,419,521 MAP2K1
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