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Items: 1 to 20 of 1794

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6122598copy number variation1nstd186human GRCh37 chr10: 11,325,823-11,326,466 , GRCh38.p12 chr10: 11,283,860-11,284,503 CELF2
    nsv5959278insertion1nstd209human GRCh38 chr10: 11,262,940-11,262,940 , GRCh37.p13 chr10: 11,304,903-11,304,903 CELF2
    nsv5956627insertion1nstd209human GRCh38 chr10: 10,792,060-10,792,060 , GRCh37.p13 chr10: 10,834,023-10,834,023 CELF2, SFTA1P
    nsv5950145insertion1nstd209human GRCh38 chr10: 10,913,553-10,913,553 , GRCh37.p13 chr10: 10,955,516-10,955,516 CELF2
    nsv5948606insertion1nstd209human GRCh38 chr10: 10,573,778-10,573,778 , GRCh37.p13 chr10: 10,615,741-10,615,741 CELF2
    nsv5926288copy number variation1nstd209human GRCh38 chr10: 10,620,786-10,621,119 , GRCh37.p13 chr10: 10,662,749-10,663,082 CELF2
    nsv5925750copy number variation1nstd209human GRCh38 chr10: 11,283,955-11,284,010 , GRCh37.p13 chr10: 11,325,918-11,325,973 CELF2
    nsv5924767copy number variation1nstd209human GRCh38 chr10: 10,767,840-10,768,009 , GRCh37.p13 chr10: 10,809,803-10,809,972 CELF2
    nsv5923466copy number variation1nstd209human GRCh38 chr10: 10,939,075-10,939,198 , GRCh37.p13 chr10: 10,981,038-10,981,161 CELF2, LINC00710
    nsv5921109copy number variation1nstd209human GRCh38 chr10: 11,285,804-11,286,420 , GRCh37.p13 chr10: 11,327,767-11,328,383 CELF2
    nsv5916618copy number variation1nstd209human GRCh38 chr10: 10,666,580-10,666,896 , GRCh37.p13 chr10: 10,708,543-10,708,859 CELF2
    nsv5913482copy number variation1nstd209human GRCh38 chr10: 11,022,229-11,023,616 , GRCh37.p13 chr10: 11,064,192-11,065,579 CELF2
    nsv5911936copy number variation1nstd209human GRCh38 chr10: 11,111,883-11,115,050 , GRCh37.p13 chr10: 11,153,846-11,157,013 CELF2
    nsv5909758copy number variation1nstd209human GRCh38 chr10: 10,471,041-10,472,420 , GRCh37.p13 chr10: 10,513,004-10,514,383 CELF2
    nsv5909532copy number variation1nstd209human GRCh38 chr10: 10,614,088-10,619,048 , GRCh37.p13 chr10: 10,656,051-10,661,011 CELF2
    nsv5867043copy number variation1nstd209human GRCh38 chr10: 11,111,961-11,115,060 , GRCh37.p13 chr10: 11,153,924-11,157,023 CELF2
    nsv5865782copy number variation1nstd209human GRCh38 chr10: 11,022,337-11,023,636 , GRCh37.p13 chr10: 11,064,300-11,065,599 CELF2
    nsv5852686copy number variation1nstd209human GRCh38 chr10: 10,614,060-10,618,958 , GRCh37.p13 chr10: 10,656,023-10,660,921 CELF2
    nsv5711686mobile element insertion1nstd211human GRCh38 chr10: 11,001,354-11,001,354 , GRCh37.p13 chr10: 11,043,317-11,043,317 CELF2
    nsv5709091mobile element insertion1nstd211human GRCh38 chr10: 10,770,719-10,770,719 , GRCh37.p13 chr10: 10,812,682-10,812,682 CELF2
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