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Items: 1 to 20 of 264

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5885360copy number variation1nstd209human GRCh38 chr2: 60,976,565-61,000,114 , GRCh37.p13 chr2: 61,203,700-61,227,249 RNA5SP95, PUS10
    nsv5884904copy number variation1nstd209human GRCh38 chr2: 60,974,048-60,974,103 , GRCh37.p13 chr2: 61,201,183-61,201,238 PUS10
    nsv5883786copy number variation1nstd209human GRCh38 chr2: 60,982,757-60,986,074 , GRCh37.p13 chr2: 61,209,892-61,213,209 PUS10
    nsv5833672copy number variation1nstd209human GRCh38 chr2: 60,988,482-60,999,565 , GRCh37.p13 chr2: 61,215,617-61,226,700 PUS10, RNA5SP95
    nsv5833435copy number variation1nstd209human GRCh38 chr2: 60,976,606-60,985,066 , GRCh37.p13 chr2: 61,203,741-61,212,201 PUS10
    nsv5833080copy number variation2nstd209human GRCh38 chr2: 60,984,377-60,985,916 , GRCh37.p13 chr2: 61,211,512-61,213,051 PUS10
    nsv5833079copy number variation2nstd209human GRCh38 chr2: 60,982,877-60,985,416 , GRCh37.p13 chr2: 61,210,012-61,212,551 PUS10
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5443447copy number variation1nstd206human GRCh38 chr2: 60,993,418-60,994,269 , GRCh37.p13 chr2: 61,220,553-61,221,404 PUS10
    nsv5360484translocation1nstd200human GRCh38 chr2: 61,003,555-61,003,555 , GRCh38 chr2: 61,003,614-61,003,614 , GRCh37.p13 chr2: 61,230,690-61,230,690 , GRCh37.p13 chr2: 61,230,749-61,230,749 PUS10
    nsv5360480translocation1nstd200human GRCh38 chr2: 60,972,610-60,972,610 , GRCh38 chr2: 60,982,674-60,982,674 , GRCh37.p13 chr2: 61,199,745-61,199,745 , GRCh37.p13 chr2: 61,209,809-61,209,809 PUS10
    nsv5068600mobile element insertion1nstd203human GRCh38 chr2: 60,991,671-60,991,684 , GRCh37.p13 chr2: 61,218,806-61,218,819 PUS10
    nsv5030307inversion1nstd200human GRCh38 chr2: 48,550,793-61,622,055 , GRCh37.p13 chr2: 48,777,932-61,849,190 , MIR217, 146 more genes
    nsv4901458copy number variation1nstd200human GRCh38 chr2: 60,987,666-60,993,346 , GRCh37.p13 chr2: 61,214,801-61,220,481 PUS10
    nsv4901457copy number variation1nstd200human GRCh38 chr2: 60,983,106-60,986,161 , GRCh37.p13 chr2: 61,210,241-61,213,296 PUS10
    nsv4901456copy number variation1nstd200human GRCh38 chr2: 60,950,636-60,975,296 , GRCh37.p13 chr2: 61,177,771-61,202,431 PUS10
    nsv4770371copy number variation1nstd200human GRCh37 chr2: 61,210,241-61,213,296 , GRCh38.p12 chr2: 60,983,106-60,986,161 PUS10
    nsv4584051copy number variation1nstd183human GRCh37 chr2: 61,236,021-61,237,143 , GRCh38.p12 chr2: 61,008,886-61,010,008 PUS10
    nsv4561623mobile element insertion1nstd166human GRCh37.p13 chr2: 61,171,927-61,171,927 , GRCh38.p12 chr2: 60,944,792-60,944,792 PUS10
    nsv4533631insertion1nstd166human GRCh37.p13 chr2: 61,209,030-61,209,030 , GRCh38.p12 chr2: 60,981,895-60,981,895 PUS10
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