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Items: 1 to 20 of 1733

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1398456copy number variation5nstd102humanPathogenic GRCh38 chr1: 155,235,750-155,235,804 , GRCh37 chr1: 155,205,541-155,205,595 GBA1
    nsv3899743copy number variation1nstd102humanBenign GRCh37 chr12: 125,024,748-125,026,411 , GRCh38.p12 chr12: 124,540,202-124,541,865 NCOR2
    nsv3898924copy number variation1nstd102humanBenign GRCh37 chr12: 125,024,848-125,030,170 , GRCh38.p12 chr12: 124,540,302-124,545,624 NCOR2
    nsv3897698copy number variation1nstd102humanBenign GRCh37 chr12: 125,025,004-125,029,775 , GRCh38.p12 chr12: 124,540,458-124,545,229 NCOR2
    nsv3893863copy number variation1nstd102humanBenign GRCh37 chr12: 125,025,004-125,026,411 , GRCh38.p12 chr12: 124,540,458-124,541,865 NCOR2
    esv4008396copy number variation1estd231human GRCh37 chr12: 124,923,368-124,923,965 , GRCh38.p12 chr12: 124,438,822-124,439,419 NCOR2
    nsv6918872copy number variation1nstd229human GRCh38 chr12: 124,404,844-124,412,564 , GRCh37.p13 chr12: 124,889,390-124,897,110 NCOR2
    nsv6988713copy number variation1nstd229human GRCh38 chr17: 46,002,190-46,009,634 , GRCh37.p13 chr17: 44,079,556-44,087,000 MAPT
    nsv6931359copy number variation1nstd229human GRCh38 chr12: 124,390,549-124,397,622 , GRCh37.p13 chr12: 124,875,095-124,882,168 NCOR2
    nsv6989602copy number variation1nstd229human GRCh38 chr17: 46,003,793-46,008,963 , GRCh37.p13 chr17: 44,081,159-44,086,329 MAPT
    nsv6930091copy number variation1nstd229human GRCh38 chr12: 124,409,640-124,414,687 , GRCh37.p13 chr12: 124,894,186-124,899,233 NCOR2
    nsv6920460copy number variation1nstd229human GRCh38 chr12: 124,366,175-124,370,947 , GRCh37.p13 chr12: 124,850,721-124,855,493 NCOR2
    nsv6986038copy number variation1nstd229human GRCh38 chr17: 46,001,901-46,006,000 , GRCh37.p13 chr17: 44,079,267-44,083,366 MAPT
    nsv6925800copy number variation1nstd229human GRCh38 chr12: 124,364,926-124,368,518 , GRCh37.p13 chr12: 124,849,472-124,853,064 NCOR2
    nsv6986843copy number variation1nstd229human GRCh38 chr17: 45,952,401-45,955,400 , GRCh37.p13 chr17: 44,029,767-44,032,766 MAPT
    nsv6925702copy number variation1nstd229human GRCh38 chr12: 124,488,999-124,491,793 , GRCh37.p13 chr12: 124,973,545-124,976,339 NCOR2
    nsv6933825copy number variation1nstd229human GRCh38 chr12: 124,529,201-124,531,400 , GRCh37.p13 chr12: 125,013,747-125,015,946 NCOR2
    nsv6933183copy number variation1nstd229human GRCh38 chr12: 124,358,550-124,359,935 , GRCh37.p13 chr12: 124,843,096-124,844,481 NCOR2
    nsv6919199copy number variation1nstd229human GRCh38 chr12: 124,371,668-124,372,499 , GRCh37.p13 chr12: 124,856,214-124,857,045 NCOR2
    nsv6989078copy number variation1nstd229human GRCh38 chr17: 45,958,913-45,959,674 , GRCh37.p13 chr17: 44,036,279-44,037,040 MAPT
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