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Items: 1 to 20 of 379

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923742copy number variation1nstd209human GRCh38 chr12: 21,398,810-28,763,815 , GRCh37.p13 chr12: 21,551,744-28,916,748 , LOC105369710, 101 more genes
    nsv5918123copy number variation1nstd209human GRCh38 chr12: 27,495,209-27,502,229 , GRCh37.p13 chr12: 27,648,142-27,655,162 RARS1P1, SMCO2
    nsv5916901copy number variation1nstd209human GRCh38 chr12: 21,398,719-28,763,765 , GRCh37.p13 chr12: 21,551,653-28,916,698 , LOC105369704, 101 more genes
    nsv5912980copy number variation1nstd209human GRCh38 chr12: 25,481,034-28,003,055 , GRCh37.p13 chr12: 25,633,968-28,155,988 , ITPR2-AS1, 36 more genes
    nsv5860995copy number variation1nstd209human GRCh38 chr12: 27,495,184-27,499,984 , GRCh37.p13 chr12: 27,648,117-27,652,917 SMCO2, RARS1P1
    nsv5596187copy number variation1nstd207human GRCh38 chr12: 27,495,209-27,502,229 , GRCh37.p13 chr12: 27,648,142-27,655,162 RARS1P1, SMCO2
    nsv5512857copy number variation1nstd206human GRCh38 chr12: 27,495,210-27,502,230 , GRCh37.p13 chr12: 27,648,143-27,655,163 SMCO2, RARS1P1
    nsv5498428copy number variation1nstd206human GRCh38 chr12: 27,130,650-27,643,000 , GRCh37.p13 chr12: 27,283,583-27,795,933 PPFIBP1, STK38L, 5 more genes
    nsv5389892copy number variation2nstd186human GRCh37 chr12: 27,648,143-27,655,163 , GRCh38.p12 chr12: 27,495,210-27,502,230 RARS1P1, SMCO2
    nsv5303075copy number variation1nstd204human GRCh37.p13 chr12: 27,648,142-27,655,163 , GRCh38.p13 chr12: 27,495,209-27,502,230 RARS1P1, SMCO2
    nsv5277003copy number variation1nstd204human GRCh38.p13 chr12: 27,494,984-27,496,083 , GRCh37.p13 chr12: 27,647,917-27,649,016 SMCO2, RARS1P1
    nsv5271578copy number variation1nstd204human GRCh38.p13 chr12: 27,495,959-27,501,042 , GRCh37.p13 chr12: 27,648,892-27,653,975 RARS1P1, SMCO2
    nsv5265572copy number variation1nstd204human GRCh38.p13 chr12: 27,495,201-27,502,200 , GRCh37.p13 chr12: 27,648,134-27,655,133 RARS1P1, SMCO2
    nsv5264070copy number variation1nstd204human GRCh38.p13 chr12: 27,468,000-27,495,283 , GRCh37.p13 chr12: 27,620,933-27,648,216 SMCO2, RARS1P1
    nsv5261840copy number variation1nstd204human GRCh38.p13 chr12: 27,494,347-27,501,998 , GRCh37.p13 chr12: 27,647,280-27,654,931 SMCO2, RARS1P1
    nsv4981689copy number variation1nstd200human GRCh38 chr12: 27,498,826-27,510,745 , GRCh37.p13 chr12: 27,651,759-27,663,678 RARS1P1, SMCO2
    nsv4981688copy number variation1nstd200human GRCh38 chr12: 27,495,210-27,502,230 , GRCh37.p13 chr12: 27,648,143-27,655,163 SMCO2, RARS1P1
    nsv4981677copy number variation1nstd200human GRCh38 chr12: 27,132,159-27,644,274 , GRCh37.p13 chr12: 27,285,092-27,797,207 PPFIBP1, STK38L, 5 more genes
    nsv4844488copy number variation1nstd200human GRCh37 chr12: 27,648,143-27,655,163 , GRCh38.p12 chr12: 27,495,210-27,502,230 SMCO2, RARS1P1
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
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