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Items: 1 to 20 of 310

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977321insertion1nstd209human GRCh38 chr12: 133,205,173-133,205,173 , GRCh37.p13 chr12: 133,781,759-133,781,759 ZNF268
    nsv5969700insertion1nstd209human GRCh38 chr12: 133,185,497-133,185,497 , GRCh37.p13 chr12: 133,762,083-133,762,083 ZNF268
    nsv5946463copy number variation1nstd209human GRCh38 chr12: 133,194,919-133,195,070 , GRCh37.p13 chr12: 133,771,505-133,771,656 ZNF268
    nsv5936903copy number variation1nstd209human GRCh38 chr12: 132,943,180-133,182,732 , GRCh37.p13 chr12: 133,519,766-133,759,318 ZNF84-DT, ZNF891, 10 more genes
    nsv5936503copy number variation1nstd209human GRCh38 chr12: 133,111,291-133,240,412 , GRCh37.p13 chr12: 133,687,877-133,816,998 ZNF10, ZNF268, 4 more genes
    nsv5932789copy number variation1nstd209human GRCh38 chr12: 133,101,121-133,186,346 , GRCh37.p13 chr12: 133,677,707-133,762,932 ZNF140, ZNF10, 3 more genes
    nsv5867244copy number variation2nstd209human GRCh38 chr12: 133,178,291-133,180,814 , GRCh37.p13 chr12: 133,754,877-133,757,400 ZNF268
    nsv5866690copy number variation2nstd209human GRCh38 chr12: 133,209,695-133,216,265 , GRCh37.p13 chr12: 133,786,281-133,792,851 ZNF268
    nsv5865182copy number variation2nstd209human GRCh38 chr12: 133,201,913-133,206,141 , GRCh37.p13 chr12: 133,778,499-133,782,727 ZNF268
    nsv5862352copy number variation2nstd209human GRCh38 chr12: 133,204,913-133,212,394 , GRCh37.p13 chr12: 133,781,499-133,788,980 ZNF268
    nsv5861566copy number variation2nstd209human GRCh38 chr12: 133,178,191-133,189,414 , GRCh37.p13 chr12: 133,754,777-133,766,000 ZNF268
    nsv5860685copy number variation2nstd209human GRCh38 chr12: 133,208,242-133,209,494 , GRCh37.p13 chr12: 133,784,828-133,786,080 ZNF268
    nsv5859818copy number variation2nstd209human GRCh38 chr12: 133,206,342-133,209,494 , GRCh37.p13 chr12: 133,782,928-133,786,080 ZNF268
    nsv5858945copy number variation2nstd209human GRCh38 chr12: 133,192,115-133,194,714 , GRCh37.p13 chr12: 133,768,701-133,771,300 ZNF268
    nsv5858496copy number variation2nstd209human GRCh38 chr12: 133,193,515-133,197,132 , GRCh37.p13 chr12: 133,770,101-133,773,718 ZNF268
    nsv5858259copy number variation2nstd209human GRCh38 chr12: 133,207,942-133,210,694 , GRCh37.p13 chr12: 133,784,528-133,787,280 ZNF268
    nsv5856975copy number variation2nstd209human GRCh38 chr12: 133,199,739-133,201,212 , GRCh37.p13 chr12: 133,776,325-133,777,798 ZNF268
    nsv5856619copy number variation2nstd209human GRCh38 chr12: 133,193,115-133,196,432 , GRCh37.p13 chr12: 133,769,701-133,773,018 ZNF268
    nsv5856496copy number variation2nstd209human GRCh38 chr12: 133,213,316-133,219,315 , GRCh37.p13 chr12: 133,789,902-133,795,901 ZNF268, ANHX
    nsv5855320copy number variation2nstd209human GRCh38 chr12: 133,183,515-133,186,514 , GRCh37.p13 chr12: 133,760,101-133,763,100 ZNF268
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