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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094683copy number variation1nstd102humanUncertain significance GRCh37 chr16: 65,821,800-72,146,396 , GRCh38.p12 chr16: 65,787,897-72,112,497 TRG-GCC5-1, RNU6-359P, 205 more genes
    nsv7094682copy number variation2nstd102humanPathogenic GRCh37 chr16: 65,821,800-67,208,957 , GRCh38.p12 chr16: 65,787,897-67,175,054 RNA5SP428, PHAF1, 38 more genes
    nsv6996768copy number variation1nstd229human GRCh38 chr16: 66,941,513-66,941,639 , GRCh37.p13 chr16: 66,975,416-66,975,542 CES2
    nsv6990340copy number variation1nstd229human GRCh38 chr16: 66,732,301-67,029,000 , GRCh37.p13 chr16: 66,766,204-67,062,903 DYNC1LI2-DT, NAE1, 14 more genes
    nsv6990199copy number variation1nstd229human GRCh38 chr16: 66,934,711-66,938,174 , GRCh37.p13 chr16: 66,968,614-66,972,077 CIAO2B, CES2
    nsv6981596copy number variation1nstd229human GRCh38 chr16: 66,940,488-67,029,327 , GRCh37.p13 chr16: 66,974,391-67,063,230 LOC107984881, CES2, 4 more genes
    nsv6979396copy number variation1nstd229human GRCh38 chr16: 66,841,465-67,115,793 , GRCh37.p13 chr16: 66,875,368-67,149,696 CBFB, CDH16, 11 more genes
    nsv6508640copy number variation1nstd223human GRCh38 chr16: 66,934,707-66,938,169 , GRCh37.p13 chr16: 66,968,610-66,972,072 CIAO2B, CES2
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv5927890copy number variation1nstd209human GRCh38 chr16: 66,940,488-67,029,326 , GRCh37.p13 chr16: 66,974,391-67,063,229 CBFB, CES2, 4 more genes
    nsv5887344copy number variation1nstd209human GRCh38 chr16: 66,940,257-66,948,699 , GRCh37.p13 chr16: 66,974,160-66,982,602 LOC107984881, CES2
    nsv5709050mobile element insertion1nstd211human GRCh38 chr16: 66,944,324-66,944,324 , GRCh37.p13 chr16: 66,978,227-66,978,227 CES2
    nsv5532815copy number variation1nstd206human GRCh38 chr16: 66,940,488-67,029,328 , GRCh37.p13 chr16: 66,974,391-67,063,231 CBFB, CES2, 4 more genes
    nsv5271075copy number variation1nstd204human GRCh38.p13 chr16: 66,941,232-66,949,831 , GRCh37.p13 chr16: 66,975,135-66,983,734 LOC107984881, CES2
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv5005777copy number variation1nstd200human GRCh38 chr16: 66,940,488-67,029,328 , GRCh37.p13 chr16: 66,974,391-67,063,231 CES3, LOC107984881, 4 more genes
    nsv5005776copy number variation1nstd200human GRCh38 chr16: 66,935,725-66,948,986 , GRCh37.p13 chr16: 66,969,628-66,982,889 LOC107984881, CES2
    nsv4993079copy number variation1nstd200human GRCh38 chr16: 66,936,022-66,948,988 , GRCh37.p13 chr16: 66,969,925-66,982,891 CES2, LOC107984881
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
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