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Items: 1 to 20 of 158

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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
    nsv6992007copy number variation1nstd229human GRCh38 chr16: 66,971,816-66,981,490 , GRCh37.p13 chr16: 67,005,719-67,015,393 CES3
    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
    nsv6989050copy number variation1nstd229human GRCh38 chr16: 66,962,183-66,967,676 , GRCh37.p13 chr16: 66,996,086-67,001,579 CES3
    nsv6986833copy number variation1nstd229human GRCh38 chr16: 66,964,395-66,997,463 , GRCh37.p13 chr16: 66,998,298-67,031,366 CES4A, CES3
    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
    nsv6506048copy number variation1nstd223human GRCh38 chr16: 66,961,832-66,968,343 , GRCh37.p13 chr16: 66,995,735-67,002,246 CES3
    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
    nsv6144974copy number variation1nstd206human GRCh38 chr16: 66,961,759-66,968,411 , GRCh37.p13 chr16: 66,995,662-67,002,314 CES3
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv5935871copy number variation1nstd209human GRCh38 chr16: 66,968,419-66,970,358 , GRCh37.p13 chr16: 67,002,322-67,004,261 CES3
    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
    nsv5883990copy number variation1nstd209human GRCh38 chr16: 66,962,013-66,964,712 , GRCh37.p13 chr16: 66,995,916-66,998,615 CES3
    nsv5882913copy number variation2nstd209human GRCh38 chr16: 66,968,581-66,969,825 , GRCh37.p13 chr16: 67,002,484-67,003,728 CES3
    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
    nsv5518218copy number variation1nstd206human GRCh38 chr16: 66,964,312-66,964,754 , GRCh37.p13 chr16: 66,998,215-66,998,657 CES3
    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
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