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Items: 1 to 20 of 558

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967638inversion1nstd209human GRCh38 chr2: 8,152,748-8,153,079 , GRCh37.p13 chr2: 8,292,878-8,293,209 LINC00299
    nsv5961484insertion1nstd209human GRCh38 chr2: 8,063,970-8,063,970 , GRCh37.p13 chr2: 8,204,100-8,204,100 LINC00299
    nsv5951838insertion1nstd209human GRCh38 chr2: 8,224,489-8,224,489 , GRCh37.p13 chr2: 8,364,619-8,364,619 LINC00299
    nsv5885893copy number variation1nstd209human GRCh38 chr2: 8,125,707-8,127,738 , GRCh37.p13 chr2: 8,265,837-8,267,868 LINC00299
    nsv5874710copy number variation1nstd209human GRCh38 chr2: 8,272,292-8,277,655 , GRCh37.p13 chr2: 8,412,422-8,417,785 LINC00299
    nsv5872487copy number variation1nstd209human GRCh38 chr2: 8,107,174-8,110,263 , GRCh37.p13 chr2: 8,247,304-8,250,393 LINC00299
    nsv5867617copy number variation1nstd209human GRCh38 chr2: 8,269,592-8,269,645 , GRCh37.p13 chr2: 8,409,722-8,409,775 LINC00299
    nsv5833822copy number variation1nstd209human GRCh38 chr2: 8,272,242-8,280,980 , GRCh37.p13 chr2: 8,412,372-8,421,110 LINC00299
    nsv5833751copy number variation1nstd209human GRCh38 chr2: 8,272,692-8,277,630 , GRCh37.p13 chr2: 8,412,822-8,417,760 LINC00299
    nsv5833746copy number variation1nstd209human GRCh38 chr2: 8,125,697-8,127,772 , GRCh37.p13 chr2: 8,265,827-8,267,902 LINC00299
    nsv5833743copy number variation1nstd209human GRCh38 chr2: 8,107,045-8,110,194 , GRCh37.p13 chr2: 8,247,175-8,250,324 LINC00299
    nsv5720762mobile element insertion1nstd211human GRCh38 chr2: 8,029,735-8,029,735 , GRCh37.p13 chr2: 8,169,865-8,169,865 LINC00299
    nsv5692518mobile element insertion1nstd211human GRCh38 chr2: 8,243,152-8,243,152 , GRCh37.p13 chr2: 8,383,282-8,383,282 LINC00299
    nsv5692467mobile element insertion2nstd211human GRCh38 chr2: 8,285,915-8,285,915 , GRCh37.p13 chr2: 8,426,045-8,426,045 LINC00299
    nsv5684277mobile element insertion2nstd211human GRCh38 chr2: 8,063,985-8,063,985 , GRCh37.p13 chr2: 8,204,115-8,204,115 LINC00299
    nsv5679807mobile element insertion2nstd211human GRCh38 chr2: 8,165,134-8,165,134 , GRCh37.p13 chr2: 8,305,264-8,305,264 LINC00299
    nsv5618395insertion1nstd207human GRCh38 chr2: 8,063,970-8,063,970 , GRCh37.p13 chr2: 8,204,100-8,204,100 LINC00299
    nsv5615501insertion2nstd207human GRCh38 chr2: 8,067,973-8,067,973 , GRCh37.p13 chr2: 8,208,103-8,208,103 LINC00299
    nsv5584381copy number variation1nstd207human GRCh38 chr2: 8,028,319-8,028,383 , GRCh37.p13 chr2: 8,168,449-8,168,513 LINC00299
    nsv5582448copy number variation1nstd207human GRCh38 chr2: 8,125,707-8,127,738 , GRCh37.p13 chr2: 8,265,837-8,267,868 LINC00299
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