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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073020inversion1nstd229human GRCh38 chr12: 96,481,691-98,593,227 , GRCh37.p13 chr12: 96,875,469-98,987,005 TRW-CCA4-1, LINC02409, 26 more genes
    nsv7068027inversion1nstd229human GRCh38 chr12: 97,559,250-97,569,650 , GRCh37.p13 chr12: 97,953,028-97,963,428 RMST, MIR135A2
    nsv7066169inversion1nstd229human GRCh38 chr12: 97,539,493-97,539,588 , GRCh37.p13 chr12: 97,933,271-97,933,366 RMST
    nsv7064866inversion1nstd229human GRCh38 chr12: 97,421,900-98,025,255 , GRCh37.p13 chr12: 97,815,678-98,419,033 MIR135A2, RMST, 5 more genes
    nsv6935517copy number variation1nstd229human GRCh38 chr12: 97,561,806-97,562,170 , GRCh37.p13 chr12: 97,955,584-97,955,948 MIR135A2, RMST
    nsv6933742copy number variation1nstd229human GRCh38 chr12: 97,522,708-97,527,358 , GRCh37.p13 chr12: 97,916,486-97,921,136 RMST
    nsv6932545copy number variation1nstd229human GRCh38 chr12: 97,510,969-97,511,583 , GRCh37.p13 chr12: 97,904,747-97,905,361 RMST
    nsv6932217copy number variation1nstd229human GRCh38 chr12: 97,554,961-97,557,344 , GRCh37.p13 chr12: 97,948,739-97,951,122 RMST
    nsv6931755copy number variation1nstd229human GRCh38 chr12: 97,523,830-97,524,070 , GRCh37.p13 chr12: 97,917,608-97,917,848 RMST
    nsv6930665copy number variation1nstd229human GRCh38 chr12: 97,525,301-97,527,800 , GRCh37.p13 chr12: 97,919,079-97,921,578 RMST
    nsv6930547copy number variation1nstd229human GRCh38 chr12: 97,553,213-97,553,235 , GRCh37.p13 chr12: 97,946,991-97,947,013 RMST
    nsv6922635copy number variation1nstd229human GRCh38 chr12: 96,115,345-104,800,221 , GRCh37.p13 chr12: 96,509,123-105,193,999 RNY1P16, CHST11, 121 more genes
    nsv6918436copy number variation1nstd229human GRCh38 chr12: 97,525,297-97,527,873 , GRCh37.p13 chr12: 97,919,075-97,921,651 RMST
    nsv6622098copy number variation1nstd224human GRCh37 chr12: 96,914,613-97,927,063 , GRCh38.p12 chr12: 96,520,835-97,533,285 RMST, LOC105369928, 9 more genes
    nsv6474589copy number variation1nstd223human GRCh38 chr12: 97,525,297-97,527,869 , GRCh37.p13 chr12: 97,919,075-97,921,647 RMST
    nsv6472617copy number variation1nstd223human GRCh38 chr12: 97,470,943-97,471,496 , GRCh37.p13 chr12: 97,864,721-97,865,274 RMST
    nsv6472256copy number variation1nstd223human GRCh38 chr12: 97,465,501-97,468,900 , GRCh37.p13 chr12: 97,859,279-97,862,678 RMST
    nsv6471047copy number variation1nstd223human GRCh38 chr12: 97,468,101-97,469,500 , GRCh37.p13 chr12: 97,861,879-97,863,278 RMST
    nsv6470853copy number variation1nstd223human GRCh38 chr12: 97,554,961-97,557,341 , GRCh37.p13 chr12: 97,948,739-97,951,119 RMST
    nsv6469323copy number variation1nstd223human GRCh38 chr12: 97,499,937-97,500,726 , GRCh37.p13 chr12: 97,893,715-97,894,504 RMST
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