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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6793479copy number variation1nstd229human GRCh38 chr5: 132,765,786-132,771,130 , GRCh37.p13 chr5: 132,101,478-132,106,822 SEPTIN8
    nsv6269806copy number variation1nstd214human GRCh38 chr5: 132,770,059-132,770,148 , GRCh37.p13 chr5: 132,105,751-132,105,840 SEPTIN8
    nsv6266426copy number variation1nstd214human GRCh38 chr5: 132,770,061-132,770,148 , GRCh37.p13 chr5: 132,105,753-132,105,840 SEPTIN8
    nsv6175667copy number variation1nstd214human GRCh38 chr5: 132,770,063-132,770,150 , GRCh37.p13 chr5: 132,105,755-132,105,842 SEPTIN8
    nsv6269059copy number variation1nstd214human GRCh38 chr5: 132,770,063-132,770,148 , GRCh37.p13 chr5: 132,105,755-132,105,840 SEPTIN8
    nsv6183920copy number variation1nstd214human GRCh38 chr5: 132,770,081-132,770,162 , GRCh37.p13 chr5: 132,105,773-132,105,854 SEPTIN8
    nsv6168028copy number variation1nstd214human GRCh38 chr5: 132,770,081-132,770,150 , GRCh37.p13 chr5: 132,105,773-132,105,842 SEPTIN8
    nsv6267892copy number variation1nstd214human GRCh38 chr5: 132,770,081-132,770,148 , GRCh37.p13 chr5: 132,105,773-132,105,840 SEPTIN8
    nsv6267273copy number variation1nstd214human GRCh38 chr5: 132,770,063-132,770,130 , GRCh37.p13 chr5: 132,105,755-132,105,822 SEPTIN8
    nsv6002671copy number variation1nstd212human GRCh38 chr5: 132,770,063-132,770,151 , GRCh37.p13 chr5: 132,105,755-132,105,843 SEPTIN8
    nsv6002394copy number variation1nstd212human GRCh38 chr5: 132,770,025-132,770,089 , GRCh37.p13 chr5: 132,105,717-132,105,781 SEPTIN8
    nsv4733661copy number variation1nstd199human GRCh37 chr5: 132,105,756-132,105,836 , GRCh38.p12 chr5: 132,770,064-132,770,144 SEPTIN8
    nsv5570404copy number variation1nstd207human GRCh38 chr5: 132,770,061-132,770,148 , GRCh37.p13 chr5: 132,105,753-132,105,840 SEPTIN8
    nsv4123518copy number variation1nstd166human GRCh37.p13 chr5: 132,091,656-132,094,528 , GRCh38.p12 chr5: 132,755,964-132,758,836 SEPTIN8
    nsv4128870copy number variation1nstd166human GRCh37.p13 chr5: 132,111,590-132,111,773 , GRCh38.p12 chr5: 132,775,898-132,776,081 SEPTIN8
    nsv3525604copy number variation3nstd152human GRCh38 chr5: 132,770,063-132,770,149 , GRCh37.p13 chr5: 132,105,755-132,105,841 SEPTIN8
    nsv3289127copy number variation1nstd152human GRCh38 chr5: 132,770,053-132,770,137 , GRCh37.p13 chr5: 132,105,745-132,105,829 SEPTIN8
    nsv3284308copy number variation1nstd152human GRCh38 chr5: 132,770,055-132,770,137 , GRCh37.p13 chr5: 132,105,747-132,105,829 SEPTIN8
    nsv3385153copy number variation5nstd162human GRCh38 chr5: 132,770,017-132,770,112 , GRCh37.p13 chr5: 132,105,709-132,105,804 SEPTIN8
    nsv3381309copy number variation1nstd162human GRCh38 chr5: 132,770,103-132,770,186 , GRCh37.p13 chr5: 132,105,795-132,105,878 SEPTIN8
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