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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7063256inversion1nstd229human GRCh38 chr12: 25,590,859-27,919,674 , GRCh37.p13 chr12: 25,743,793-28,072,607 RARS1P1, LOC101929091, 34 more genes
    nsv7062447inversion1nstd229human GRCh38 chr12: 27,083,620-27,083,645 , GRCh37.p13 chr12: 27,236,553-27,236,578 C12orf71
    nsv6935727copy number variation1nstd229human GRCh38 chr12: 27,068,078-27,080,331 , GRCh37.p13 chr12: 27,221,011-27,233,264 C12orf71
    nsv6935087copy number variation1nstd229human GRCh38 chr12: 26,967,401-27,843,600 , GRCh37.p13 chr12: 27,120,334-27,996,533 RARS1P1, RN7SKP15, 16 more genes
    nsv6934275copy number variation1nstd229human GRCh38 chr12: 27,074,759-27,083,148 , GRCh37.p13 chr12: 27,227,692-27,236,081 C12orf71
    nsv6925715copy number variation1nstd229human GRCh38 chr12: 27,083,154-27,083,234 , GRCh37.p13 chr12: 27,236,087-27,236,167 C12orf71
    nsv6924237copy number variation1nstd229human GRCh38 chr12: 27,052,517-27,217,887 , GRCh37.p13 chr12: 27,205,450-27,370,820 C12orf71
    nsv6921803copy number variation1nstd229human GRCh38 chr12: 27,080,366-27,086,196 , GRCh37.p13 chr12: 27,233,299-27,239,129 C12orf71
    nsv6920049copy number variation1nstd229human GRCh38 chr12: 27,065,701-27,102,000 , GRCh37.p13 chr12: 27,218,634-27,254,933 C12orf71
    nsv6467685copy number variation1nstd223human GRCh38 chr12: 27,068,077-27,080,330 , GRCh37.p13 chr12: 27,221,010-27,233,263 C12orf71
    nsv6458417copy number variation1nstd223human GRCh38 chr12: 27,080,366-27,086,196 , GRCh37.p13 chr12: 27,233,299-27,239,129 C12orf71
    nsv6290811copy number variation1nstd102humanPathogenic GRCh37 chr12: 23,693,737-29,545,102 , GRCh38.p12 chr12: 23,540,803-29,392,169 LOC105369709, REP15, 74 more genes
    nsv6132683copy number variation1nstd213human GRCh37 chr12: 23,270,000-28,660,001 , GRCh38.p12 chr12: 23,117,066-28,507,068 , IRAG2, 68 more genes
    nsv6132422copy number variation1nstd213human GRCh37 chr12: 190,000-30,830,001 , GRCh38.p12 chr12: 80,834-30,677,067 , A2M, 622 more genes
    nsv6132237copy number variation1nstd213human GRCh37 chr12: 27,020,000-28,120,001 , GRCh38.p12 chr12: 26,867,067-27,967,068 MED21, FGFR1OP2, 19 more genes
    nsv6132236copy number variation1nstd213human GRCh37 chr12: 27,000,000-27,840,001 , GRCh38.p12 chr12: 26,847,067-27,687,068 PPFIBP1, MED21, 10 more genes
    nsv6132235copy number variation1nstd213human GRCh37 chr12: 26,030,000-27,870,001 , GRCh38.p12 chr12: 25,877,067-27,717,068 ITPR2, RASSF8, 26 more genes
    nsv5925838copy number variation1nstd209human GRCh38 chr12: 27,083,154-27,083,233 , GRCh37.p13 chr12: 27,236,087-27,236,166 C12orf71
    nsv5923742copy number variation1nstd209human GRCh38 chr12: 21,398,810-28,763,815 , GRCh37.p13 chr12: 21,551,744-28,916,748 , LOC105369710, 101 more genes
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