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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3876706copy number variation1nstd102humanLikely pathogenic GRCh38 chr20: 42,303,583-42,488,707 , GRCh37.p13 chr20: 40,932,223-41,117,347 PTPRT
    nsv3879838copy number variation1nstd102humanLikely pathogenic GRCh38 chr20: 42,472,130-42,562,200 , GRCh37.p13 chr20: 41,100,770-41,190,840 PTPRT
    nsv3872802copy number variation1nstd102humanLikely pathogenic GRCh38 chr20: 42,232,174-42,274,201 , GRCh37.p13 chr20: 40,860,814-40,902,841 PTPRT
    nsv3897282copy number variation1nstd102humanBenign GRCh37 chr20: 41,153,263-41,222,480 , GRCh38.p12 chr20: 42,524,623-42,593,840 PTPRT
    nsv3899831copy number variation1nstd102humanBenign GRCh37 chr20: 41,179,519-41,243,236 , GRCh38.p12 chr20: 42,550,879-42,614,596 PTPRT
    nsv3893756copy number variation1nstd102humanBenign GRCh37 chr20: 41,181,630-41,241,888 , GRCh38.p12 chr20: 42,552,990-42,613,248 PTPRT
    nsv3902040copy number variation1nstd102humanBenign GRCh37 chr20: 41,613,071-41,671,118 , GRCh38.p12 chr20: 42,984,431-43,042,478 PTPRT
    nsv3896946copy number variation1nstd102humanBenign GRCh37 chr20: 41,181,630-41,235,817 , GRCh38.p12 chr20: 42,552,990-42,607,177 PTPRT
    nsv3907876copy number variation1nstd102humanBenign GRCh37 chr20: 41,202,893-41,238,504 , GRCh38.p12 chr20: 42,574,253-42,609,864 PTPRT
    nsv3902931copy number variation1nstd102humanBenign GRCh37 chr20: 41,412,936-41,439,248 , GRCh38.p12 chr20: 42,784,296-42,810,608 PTPRT
    nsv3900648copy number variation1nstd102humanBenign GRCh37 chr20: 41,168,798-41,185,138 , GRCh38.p12 chr20: 42,540,158-42,556,498 PTPRT
    nsv3920225copy number variation1nstd102humanBenign GRCh37 chr20: 41,067,417-41,107,347 , NCBI36 chr20: 40,500,831-40,540,761 , GRCh38 chr20: 42,438,777-42,478,707 PTPRT
    nsv4457738copy number variation1nstd102humanUncertain significance GRCh37 chr20: 41,403,660-41,544,992 , GRCh38.p12 chr20: 42,775,020-42,916,352 PTPRT
    nsv4729898copy number variation1nstd102humanUncertain significance GRCh37 chr20: 41,468,892-41,562,396 , GRCh38.p12 chr20: 42,840,252-42,933,756 PTPRT
    nsv3919689copy number variation1nstd102humanUncertain significance NCBI36 chr20: 40,540,761-40,613,964 , GRCh38 chr20: 42,478,707-42,551,910 , GRCh37 chr20: 41,107,347-41,180,550 PTPRT
    nsv3899612copy number variation1nstd102humanUncertain significance GRCh37 chr20: 40,938,475-40,987,033 , GRCh38.p12 chr20: 42,309,835-42,358,393 PTPRT
    nsv4457672copy number variation1nstd102humanUncertain significance GRCh37 chr20: 41,067,714-41,101,756 , GRCh38.p12 chr20: 42,439,074-42,473,116 PTPRT
    nsv3885562copy number variation1nstd102humanLikely pathogenic GRCh38 chr20: 42,461,895-42,648,116 , GRCh37.p13 chr20: 41,090,535-41,276,756 PTPRT, LOC105372624
    nsv3894985copy number variation1nstd102humanBenign GRCh37 chr20: 41,184,337-41,309,611 , GRCh38.p12 chr20: 42,555,697-42,680,971 PTPRT, LOC105372624
    nsv3896666copy number variation1nstd102humanBenign GRCh37 chr20: 41,200,266-41,302,843 , GRCh38.p12 chr20: 42,571,626-42,674,203 PTPRT, LOC105372624
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