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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5974929insertion1nstd209human GRCh38 chr16: 57,705,805-57,705,805 , GRCh37.p13 chr16: 57,739,717-57,739,717 DRC7
    nsv5940317copy number variation1nstd209human GRCh38 chr16: 57,695,742-57,697,211 , GRCh37.p13 chr16: 57,729,654-57,731,123 DRC7
    nsv5938591copy number variation1nstd209human GRCh38 chr16: 57,691,483-57,693,933 , GRCh37.p13 chr16: 57,725,395-57,727,845 DRC7
    nsv5933650copy number variation1nstd209human GRCh38 chr16: 57,689,623-57,745,532 , GRCh37.p13 chr16: 57,723,535-57,774,021 KATNB1, DRC7, 3 more genes
    nsv5932021copy number variation1nstd209human GRCh38 chr16: 57,693,734-57,693,797 , GRCh37.p13 chr16: 57,727,646-57,727,709 DRC7
    nsv5878566copy number variation2nstd209human GRCh38 chr16: 57,698,962-57,700,161 , GRCh37.p13 chr16: 57,732,874-57,734,073 DRC7
    nsv5876715copy number variation1nstd209human GRCh38 chr16: 57,691,466-57,696,117 , GRCh37.p13 chr16: 57,725,378-57,730,029 DRC7
    nsv5875312copy number variation1nstd209human GRCh38 chr16: 57,693,819-57,705,354 , GRCh37.p13 chr16: 57,727,731-57,739,266 DRC7
    nsv5870879copy number variation1nstd209human GRCh38 chr16: 57,691,465-57,693,893 , GRCh37.p13 chr16: 57,725,377-57,727,805 DRC7
    nsv5599020copy number variation1nstd207human GRCh38 chr16: 57,729,518-57,729,589 , GRCh37.p13 chr16: 57,763,430-57,763,501 DRC7
    nsv5599019copy number variation1nstd207human GRCh38 chr16: 57,706,642-57,706,736 , GRCh37.p13 chr16: 57,740,554-57,740,648 DRC7
    nsv5594446copy number variation1nstd207human GRCh38 chr16: 57,691,483-57,693,933 , GRCh37.p13 chr16: 57,725,395-57,727,845 DRC7
    nsv5589945copy number variation1nstd207human GRCh38 chr16: 57,729,109-57,729,160 , GRCh37.p13 chr16: 57,763,021-57,763,072 DRC7
    nsv5588429copy number variation1nstd207human GRCh38 chr16: 57,693,734-57,693,797 , GRCh37.p13 chr16: 57,727,646-57,727,709 DRC7
    nsv5519419copy number variation1nstd206human GRCh38 chr16: 57,691,483-57,693,934 , GRCh37.p13 chr16: 57,725,395-57,727,846 DRC7
    nsv5514271copy number variation1nstd206human GRCh38 chr16: 57,698,513-57,698,657 , GRCh37.p13 chr16: 57,732,425-57,732,569 DRC7
    nsv5309282copy number variation1nstd204human GRCh38.p13 chr16: 57,584,497-57,694,311 , GRCh37.p13 chr16: 57,618,409-57,728,223 ADGRG1, DRC7, 4 more genes
    nsv5303273copy number variation1nstd204human GRCh38.p13 chr16: 57,691,483-57,693,934 , GRCh37.p13 chr16: 57,725,395-57,727,846 DRC7
    nsv5279444copy number variation1nstd204human GRCh38.p13 chr16: 57,691,465-57,693,893 , GRCh37.p13 chr16: 57,725,377-57,727,805 DRC7
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