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Items: 1 to 20 of 279

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057108inversion1nstd229human GRCh38 chr4: 154,728,774-156,655,899 , GRCh37.p13 chr4: 155,649,926-157,577,051 RNU2-66P, LOC105377501, 38 more genes
    nsv7048230inversion1nstd229human GRCh38 chr4: 149,781,104-157,324,460 , GRCh37.p13 chr4: 150,702,256-158,245,612 LOC107986197, LINC02273, 119 more genes
    nsv6752153copy number variation1nstd229human GRCh38 chr4: 155,181,036-155,181,088 , GRCh37.p13 chr4: 156,102,188-156,102,240 NPY2R
    nsv6751799copy number variation1nstd229human GRCh38 chr4: 155,171,789-155,172,038 , GRCh37.p13 chr4: 156,092,941-156,093,190 NPY2R
    nsv6740565copy number variation1nstd229human GRCh38 chr4: 155,181,452-155,187,105 , GRCh37.p13 chr4: 156,102,604-156,108,257 NPY2R
    nsv6740248copy number variation1nstd229human GRCh38 chr4: 155,177,350-155,188,138 , GRCh37.p13 chr4: 156,098,502-156,109,290 NPY2R
    nsv6738127copy number variation1nstd229human GRCh38 chr4: 155,217,270-155,219,797 , GRCh37.p13 chr4: 156,138,422-156,140,949 NPY2R
    nsv6392968copy number variation1nstd223human GRCh38 chr4: 155,217,270-155,219,796 , GRCh37.p13 chr4: 156,138,422-156,140,948 NPY2R
    nsv6381988copy number variation1nstd223human GRCh38 chr4: 155,189,601-155,190,900 , GRCh37.p13 chr4: 156,110,753-156,112,052 NPY2R
    nsv6297659copy number variation1nstd186human GRCh37 chr4: 156,115,313-156,115,443 , GRCh38.p12 chr4: 155,194,161-155,194,291 NPY2R
    nsv6279410insertion1nstd214human GRCh38 chr4: 155,181,062-155,181,062 , GRCh37.p13 chr4: 156,102,214-156,102,214 NPY2R
    nsv6135064copy number variation1nstd213human GRCh37 chr4: 156,040,000-156,130,001 , GRCh38.p12 chr4: 155,118,848-155,208,849 NPY2R, NPY2R-AS1
    nsv6134911copy number variation1nstd213human GRCh37 chr4: 147,270,000-190,610,001 , GRCh38.p12 chr4: 146,348,848-189,688,847 , AGA, 517 more genes
    nsv6134884copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,720,001 , GRCh38.p12 chr4: 108,308,844-160,798,849 , ANK2, 616 more genes
    nsv6134731copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,710,001 , GRCh38.p12 chr4: 108,308,844-160,788,849 , ANK2, 616 more genes
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv6080311insertion1nstd212human GRCh38 chr4: 155,198,571-155,198,571 , GRCh37.p13 chr4: 156,119,723-156,119,723 NPY2R
    nsv6061853insertion1nstd212human GRCh38 chr4: 155,198,614-155,198,614 , GRCh37.p13 chr4: 156,119,766-156,119,766 NPY2R
    nsv5905685copy number variation1nstd209human GRCh38 chr4: 155,217,270-155,219,795 , GRCh37.p13 chr4: 156,138,422-156,140,947 NPY2R
    nsv5900246copy number variation1nstd209human GRCh38 chr4: 155,181,452-155,187,103 , GRCh37.p13 chr4: 156,102,604-156,108,255 NPY2R
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