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Items: 1 to 20 of 1670

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6482557copy number variation1nstd223human GRCh38 chr12: 124,366,175-124,370,943 , GRCh37.p13 chr12: 124,850,721-124,855,489 NCOR2
    nsv6506455copy number variation1nstd223human GRCh38 chr17: 45,952,368-45,955,384 , GRCh37.p13 chr17: 44,029,734-44,032,750 MAPT
    nsv6485661copy number variation1nstd223human GRCh38 chr12: 124,489,008-124,491,760 , GRCh37.p13 chr12: 124,973,554-124,976,306 NCOR2
    nsv6487117copy number variation1nstd223human GRCh38 chr12: 124,529,166-124,531,435 , GRCh37.p13 chr12: 125,013,712-125,015,981 NCOR2
    nsv6479776copy number variation1nstd223human GRCh38 chr12: 124,393,169-124,394,863 , GRCh37.p13 chr12: 124,877,715-124,879,409 NCOR2
    nsv6499865copy number variation1nstd223human GRCh38 chr17: 46,015,632-46,016,774 , GRCh37.p13 chr17: 44,092,998-44,094,140 MAPT
    nsv6488659copy number variation1nstd223human GRCh38 chr12: 124,542,937-124,543,643 , GRCh37.p13 chr12: 125,027,483-125,028,189 NCOR2
    nsv6503495copy number variation1nstd223human GRCh38 chr17: 45,947,445-45,948,068 , GRCh37.p13 chr17: 44,024,811-44,025,434 MAPT
    nsv6500849copy number variation1nstd223human GRCh38 chr17: 45,958,924-45,959,534 , GRCh37.p13 chr17: 44,036,290-44,036,900 MAPT
    nsv6502995copy number variation1nstd223human GRCh38 chr17: 45,969,410-45,969,642 , GRCh37.p13 chr17: 44,046,776-44,047,008 MAPT
    nsv6506188copy number variation1nstd223human GRCh38 chr17: 46,009,418-46,009,595 , GRCh37.p13 chr17: 44,086,784-44,086,961 MAPT
    nsv5501747copy number variation1nstd206human GRCh38 chr12: 124,367,706-124,371,002 , GRCh37.p13 chr12: 124,852,252-124,855,548 NCOR2
    nsv5505339copy number variation1nstd206human GRCh38 chr12: 124,529,166-124,531,435 , GRCh37.p13 chr12: 125,013,712-125,015,981 NCOR2
    nsv5518036copy number variation1nstd206human GRCh38 chr17: 46,016,674-46,018,101 , GRCh37.p13 chr17: 44,094,040-44,095,467 MAPT
    nsv6143478copy number variation1nstd206human GRCh38 chr12: 124,373,275-124,373,886 , GRCh37.p13 chr12: 124,857,821-124,858,432 NCOR2
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