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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5929698copy number variation1nstd209human GRCh38 chr16: 23,643,248-23,645,190 , GRCh37.p13 chr16: 23,654,569-23,656,511 DCTN5
    nsv5929387copy number variation1nstd209human GRCh38 chr16: 20,698,055-24,692,430 , GRCh37.p13 chr16: 20,709,377-24,703,751 , ACSM1, 87 more genes
    nsv5886406copy number variation1nstd209human GRCh38 chr16: 23,643,279-23,644,778 , GRCh37.p13 chr16: 23,654,600-23,656,099 DCTN5
    nsv5672923copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr16: 23,619,175-23,652,478 , GRCh38.p12 chr16: 23,607,854-23,641,157 PALB2, DCTN5
    nsv5527415copy number variation1nstd206human GRCh38 chr16: 23,665,976-23,666,052 , GRCh37.p13 chr16: 23,677,297-23,677,373 DCTN5
    nsv5517735copy number variation1nstd206human GRCh38 chr16: 23,643,030-23,645,173 , GRCh37.p13 chr16: 23,654,351-23,656,494 DCTN5
    nsv5391568copy number variation1nstd186human GRCh37 chr16: 23,654,574-23,656,494 , GRCh38.p12 chr16: 23,643,253-23,645,173 DCTN5
    nsv5349570translocation1nstd200human GRCh38 chr16: 23,666,052-23,666,052 , GRCh38 chr16: 23,665,976-23,665,976 , GRCh37.p13 chr16: 23,677,297-23,677,297 , GRCh37.p13 chr16: 23,677,373-23,677,373 DCTN5
    nsv5331811translocation1nstd200human GRCh37 chr16: 23,677,297-23,677,297 , GRCh37 chr16: 23,677,373-23,677,373 , GRCh38.p12 chr16: 23,666,052-23,666,052 , GRCh38.p12 chr16: 23,665,976-23,665,976 DCTN5
    nsv5306580copy number variation1nstd204human GRCh38.p13 chr16: 23,643,198-23,645,245 , GRCh37.p13 chr16: 23,654,519-23,656,566 DCTN5
    nsv5271974copy number variation1nstd204human GRCh38.p13 chr16: 23,643,201-23,646,000 , GRCh37.p13 chr16: 23,654,522-23,657,321 DCTN5
    nsv5261832copy number variation1nstd204human GRCh38.p13 chr16: 23,643,229-23,644,928 , GRCh37.p13 chr16: 23,654,550-23,656,249 DCTN5
    nsv5155651mobile element insertion1nstd203human GRCh38 chr16: 23,649,191-23,649,206 , GRCh37.p13 chr16: 23,660,512-23,660,527 DCTN5
    nsv5140913mobile element insertion1nstd203human GRCh38 chr16: 23,645,100-23,645,113 , GRCh37.p13 chr16: 23,656,421-23,656,434 DCTN5
    nsv5003205copy number variation1nstd200human GRCh38 chr16: 23,645,012-23,645,701 , GRCh37.p13 chr16: 23,656,333-23,657,022 DCTN5
    nsv5003204copy number variation1nstd200human GRCh38 chr16: 23,643,252-23,645,173 , GRCh37.p13 chr16: 23,654,573-23,656,494 DCTN5
    nsv4850746copy number variation1nstd200human GRCh37 chr16: 23,656,333-23,657,022 , GRCh38.p12 chr16: 23,645,012-23,645,701 DCTN5
    nsv4850745copy number variation1nstd200human GRCh37 chr16: 23,654,571-23,656,494 , GRCh38.p12 chr16: 23,643,250-23,645,173 DCTN5
    nsv4739672copy number variation1nstd199human GRCh37 chr16: 23,677,294-23,677,372 , GRCh38.p12 chr16: 23,665,973-23,666,051 DCTN5
    nsv4735217copy number variation1nstd199human GRCh37 chr16: 23,654,550-23,656,494 , GRCh38.p12 chr16: 23,643,229-23,645,173 DCTN5
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