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Items: 1 to 20 of 473

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053948inversion1nstd229human GRCh38 chr2: 236,325,891-239,580,552 , GRCh37.p13 chr2: 237,234,534-240,502,246 PER2, MIR4269, 60 more genes
    nsv7048459inversion1nstd229human GRCh38 chr2: 238,861,424-238,972,253 , GRCh37.p13 chr2: 239,770,065-239,893,949 TWIST2, LINC01940
    nsv7047549inversion1nstd229human GRCh38 chr2: 236,010,287-240,118,231 , GRCh37.p13 chr2: 236,918,931-241,057,648 RAB17, COL6A3, 74 more genes
    nsv7046600inversion1nstd229human GRCh38 chr2: 237,108,675-239,672,919 , GRCh37.p13 chr2: 238,017,318-240,594,613 RBM44, MIR4440, 46 more genes
    nsv7040475inversion1nstd229human GRCh38 chr2: 238,760,414-238,951,359 , GRCh37.p13 chr2: 239,669,055-239,873,055 TWIST2, LINC01940, 1 more genes
    nsv6716659copy number variation1nstd229human GRCh38 chr2: 238,872,463-238,876,488 , GRCh37.p13 chr2: 239,781,104-239,785,129 TWIST2
    nsv6716136copy number variation1nstd229human GRCh38 chr2: 238,760,401-238,861,400 , GRCh37.p13 chr2: 239,669,042-239,770,041 LOC100287387, TWIST2
    nsv6714706copy number variation1nstd229human GRCh38 chr2: 238,856,142-238,863,756 , GRCh37.p13 chr2: 239,764,783-239,772,397 TWIST2
    nsv6714695copy number variation1nstd229human GRCh38 chr2: 238,876,850-238,879,428 , GRCh37.p13 chr2: 239,785,491-239,788,069 TWIST2
    nsv6714295copy number variation1nstd229human GRCh38 chr2: 238,867,933-238,889,621 , GRCh37.p13 chr2: 239,776,574-239,798,262 TWIST2
    nsv6714278copy number variation1nstd229human GRCh38 chr2: 238,892,966-238,912,289 , GRCh37.p13 chr2: 239,801,607-239,833,985 TWIST2
    nsv6713801copy number variation1nstd229human GRCh38 chr2: 238,741,801-239,611,700 , GRCh37.p13 chr2: 239,650,442-240,533,394 LOC100287387, MIR2467, 10 more genes
    nsv6706169copy number variation1nstd229human GRCh38 chr2: 238,873,982-238,874,281 , GRCh37.p13 chr2: 239,782,623-239,782,922 TWIST2
    nsv6706035copy number variation1nstd229human GRCh38 chr2: 238,895,599-238,897,404 , GRCh37.p13 chr: NaN-NaN TWIST2
    nsv6704143copy number variation1nstd229human GRCh38 chr2: 238,899,374-238,905,456 , GRCh37.p13 chr: NaN-NaN TWIST2
    nsv6701995copy number variation1nstd229human GRCh38 chr2: 238,479,501-239,152,700 , GRCh37.p13 chr2: 239,388,142-240,074,396 LINC01940, MIR4440, 7 more genes
    nsv6701801copy number variation1nstd229human GRCh38 chr2: 238,908,204-238,934,612 , GRCh37.p13 chr2: 239,831,979-239,856,308 TWIST2, LINC01940
    nsv6700459copy number variation1nstd229human GRCh38 chr2: 238,886,512-238,890,274 , GRCh37.p13 chr2: 239,795,153-239,798,915 TWIST2
    nsv6699636copy number variation1nstd229human GRCh38 chr2: 238,880,031-238,944,170 , GRCh37.p13 chr2: 239,788,672-239,865,866 TWIST2, LINC01940
    nsv6636841copy number variation1nstd102humanPathogenic GRCh37 chr2: 236,878,509-242,783,384 , GRCh38.p12 chr2: 235,969,865-241,841,232 COPS8-DT, MTND5P46, 128 more genes
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