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Items: 1 to 20 of 490

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137707copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,565,626-30,221,925 , GRCh38.p12 chr16: 29,554,305-30,210,604 TAOK2, SLC7A5P1, 44 more genes
    nsv6112812copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,675,050-30,200,008 , GRCh38.p12 chr16: 29,663,729-30,188,687 INO80E, QPRT, 33 more genes
    nsv6112806copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,675,050-30,218,221 , GRCh38.p12 chr16: 29,663,729-30,206,900 YPEL3-DT, PAGR1, 38 more genes
    nsv6112788copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,615,859-30,199,454 , GRCh38.p12 chr16: 29,604,538-30,188,133 ALDOA, MVP, 36 more genes
    nsv5980454copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,545,794-30,307,472 , GRCh38.p12 chr16: 29,534,473-30,296,151 LOC105371167, MIR3680-2, 46 more genes
    nsv5944299copy number variation1nstd209human GRCh38 chr16: 30,072,078-30,074,242 , GRCh37.p13 chr16: 30,083,399-30,085,563 PPP4C
    nsv5938679copy number variation1nstd209human GRCh38 chr16: 29,576,286-30,317,646 , GRCh37.p13 chr16: 29,587,607-30,328,967 , BOLA2B, 47 more genes
    nsv5936982copy number variation1nstd209human GRCh38 chr16: 30,079,443-30,080,759 , GRCh37.p13 chr16: 30,090,764-30,092,080 PPP4C
    nsv5936291copy number variation1nstd209human GRCh38 chr16: 30,075,272-30,075,441 , GRCh37.p13 chr16: 30,086,593-30,086,762 PPP4C
    nsv5880166copy number variation1nstd209human GRCh38 chr16: 30,072,210-30,074,309 , GRCh37.p13 chr16: 30,083,531-30,085,630 PPP4C
    nsv5672756copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,675,044-30,212,202 , GRCh38.p12 chr16: 29,663,723-30,200,881 ALDOA, QPRT, 37 more genes
    nsv5564226copy number variation7nstd102humanPathogenic, Uncertain significance GRCh37 chr16: 29,802,081-30,199,917 , GRCh38.p12 chr16: 29,790,760-30,188,596 MAPK3, MAZ, 27 more genes
    nsv5524028copy number variation1nstd206human GRCh38 chr16: 30,072,115-30,074,243 , GRCh37.p13 chr16: 30,083,436-30,085,564 PPP4C
    nsv5519942copy number variation1nstd206human GRCh38 chr16: 29,446,486-30,285,000 , GRCh37.p13 chr16: 29,457,807-30,296,321 , CA5AP1, 57 more genes
    nsv5380931copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr16: 29,802,081-30,200,285 , GRCh38.p12 chr16: 29,790,760-30,188,964 CDIPTOSP, MAZ, 27 more genes
    nsv5358076translocation1nstd200human GRCh38 chr16: 30,072,114-30,072,114 , GRCh38 chr16: 30,074,243-30,074,243 , GRCh37.p13 chr16: 30,083,435-30,083,435 , GRCh37.p13 chr16: 30,085,564-30,085,564 PPP4C
    nsv5333408translocation1nstd200human GRCh37 chr16: 30,083,436-30,083,436 , GRCh37 chr16: 30,085,564-30,085,564 , GRCh38.p12 chr16: 30,074,243-30,074,243 , GRCh38.p12 chr16: 30,072,115-30,072,115 PPP4C
    nsv5278337copy number variation1nstd204human GRCh37.p13 chr16: 30,070,980-30,109,899 , GRCh38.p13 chr16: 30,059,659-30,098,578 ALDOA, PPP4C, 4 more genes
    nsv5274784copy number variation1nstd204human GRCh38.p13 chr16: 30,072,435-30,101,001 , GRCh37.p13 chr16: 30,083,756-30,112,322 PPP4C, TBX6, 2 more genes
    nsv5200388copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,652,999-30,198,600 , GRCh38.p12 chr16: 29,641,678-30,187,279 PAGR1, MVP, 33 more genes
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