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Items: 1 to 20 of 2444

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6312813copy number variation1nstd102humanPathogenic GRCh37 chr8: 141,460,869-141,461,502 , GRCh38.p12 chr8: 140,450,770-140,451,403 TRAPPC9
    nsv7097894copy number variation1nstd102humanPathogenic GRCh37 chr8: 141,034,014-141,034,196 , GRCh38.p12 chr8: 140,023,917-140,024,099 TRAPPC9
    nsv6312812copy number variation1nstd102humanPathogenic GRCh37 chr8: 141,321,327-141,321,493 , GRCh38.p12 chr8: 140,311,228-140,311,394 TRAPPC9
    nsv3874368copy number variation1nstd102humanLikely pathogenic GRCh38 chr8: 140,417,391-140,444,832 , GRCh37.p13 chr8: 141,427,490-141,454,931 TRAPPC9
    nsv3920205copy number variation1nstd102humanUncertain significance NCBI36 chr8: 141,366,732-141,472,896 , GRCh38 chr8: 140,287,451-140,393,615 , GRCh37 chr8: 141,297,550-141,403,714 TRAPPC9
    nsv6290860copy number variation1nstd102humanUncertain significance GRCh37 chr8: 141,320,475-141,375,391 , GRCh38.p12 chr8: 140,310,376-140,365,292 TRAPPC9
    nsv7097895copy number variation1nstd102humanUncertain significance GRCh37 chr8: 141,445,191-141,468,663 , GRCh38.p12 chr8: 140,435,092-140,458,564 TRAPPC9
    nsv7098164copy number variation1nstd102humanUncertain significance GRCh37 chr8: 141,468,360-141,468,663 , GRCh38.p12 chr8: 140,458,261-140,458,564 TRAPPC9
    nsv6858234copy number variation1nstd229human GRCh38 chr8: 140,108,413-140,212,579 , GRCh37.p13 chr8: 141,118,512-141,222,678 TRAPPC9
    nsv6867950copy number variation1nstd229human GRCh38 chr8: 139,926,840-140,011,774 , GRCh37.p13 chr8: 140,939,084-141,021,871 TRAPPC9
    nsv6858176copy number variation1nstd229human GRCh38 chr8: 139,807,399-139,839,234 , GRCh37.p13 chr8: 140,819,642-140,851,477 TRAPPC9
    nsv6869459copy number variation1nstd229human GRCh38 chr8: 139,948,334-139,965,142 , GRCh37.p13 chr8: 140,960,629-140,975,268 TRAPPC9
    nsv6869976copy number variation1nstd229human GRCh38 chr8: 140,042,501-140,058,700 , GRCh37.p13 chr8: 141,052,598-141,068,798 TRAPPC9
    nsv6868303copy number variation1nstd229human GRCh38 chr8: 139,966,201-139,979,300 , GRCh37.p13 chr8: 140,976,406-140,989,509 TRAPPC9
    nsv6863402copy number variation1nstd229human GRCh38 chr8: 140,323,458-140,335,187 , GRCh37.p13 chr8: 141,333,557-141,345,286 TRAPPC9
    nsv6873903copy number variation1nstd229human GRCh38 chr8: 139,925,932-139,934,962 , GRCh37.p13 chr8: 140,938,176-140,947,206 TRAPPC9
    nsv6864226copy number variation1nstd229human GRCh38 chr8: 139,739,780-139,748,529 , GRCh37.p13 chr8: 140,752,023-140,760,772 TRAPPC9
    nsv6859641copy number variation1nstd229human GRCh38 chr8: 140,328,801-140,337,100 , GRCh37.p13 chr8: 141,338,900-141,347,199 TRAPPC9
    nsv6872692copy number variation1nstd229human GRCh38 chr8: 139,789,696-139,797,126 , GRCh37.p13 chr8: 140,801,939-140,809,369 TRAPPC9
    nsv6866065copy number variation1nstd229human GRCh38 chr8: 139,729,118-139,736,318 , GRCh37.p13 chr8: 140,741,361-140,748,561 TRAPPC9
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