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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139353insertion1nstd232human GRCh37.p13 chr3: 137,881,426-137,881,426 , GRCh38.p12 chr3: 138,162,584-138,162,584 DBR1
    nsv7096539copy number variation1nstd102humanUncertain significance GRCh37 chr3: 137,880,731-137,893,637 , GRCh38.p12 chr3: 138,161,889-138,174,795 DBR1
    nsv7096443copy number variation1nstd102humanPathogenic GRCh37 chr3: 137,781,658-138,665,815 , GRCh38.p12 chr3: 138,062,816-138,946,973 ARMC8, EEF1A1P25, 17 more genes
    nsv7052094inversion1nstd229human GRCh38 chr3: 132,609,279-139,052,095 , GRCh37.p13 chr3: 132,328,123-138,770,937 RNU6-789P, UBA5, 98 more genes
    nsv7044513inversion1nstd229human GRCh38 chr3: 131,210,998-138,882,695 , GRCh37.p13 chr3: 130,929,842-138,601,537 HSPA8P9, RNU6-1174P, 114 more genes
    nsv7042471inversion1nstd229human GRCh38 chr3: 138,157,386-138,843,461 , GRCh37.p13 chr3: 137,876,228-138,562,303 FAIM, DBR1, 10 more genes
    nsv7039302inversion1nstd229human GRCh38 chr3: 133,378,933-139,551,784 , GRCh37.p13 chr3: 133,097,777-139,270,626 ESYT3, DONSONP1, 99 more genes
    nsv7039034inversion1nstd229human GRCh38 chr3: 136,134,661-138,768,814 , GRCh37.p13 chr3: 135,853,503-138,487,656 KRT8P36, RPL31P23, 37 more genes
    nsv6737901copy number variation1nstd229human GRCh38 chr3: 138,159,274-138,177,004 , GRCh37.p13 chr3: 137,878,116-137,895,846 DBR1
    nsv6728758copy number variation1nstd229human GRCh38 chr3: 138,130,649-138,217,747 , GRCh37.p13 chr3: 137,849,491-137,936,589 A4GNT, DBR1, 1 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6568954inversion1nstd223human GRCh38 chr3: 138,157,386-138,843,464 , GRCh37.p13 chr3: 137,876,228-138,562,306 NME9, FAIM, 10 more genes
    nsv6365663copy number variation1nstd223human GRCh38 chr3: 138,158,713-138,161,665 , GRCh37.p13 chr3: 137,877,555-137,880,507 DBR1
    nsv6364180copy number variation1nstd223human GRCh38 chr3: 138,159,148-138,165,684 , GRCh37.p13 chr3: 137,877,990-137,884,526 DBR1
    nsv6311778copy number variation1nstd102humanUncertain significance GRCh37 chr3: 137,781,658-139,258,560 , GRCh38.p12 chr3: 138,062,816-139,539,718 PRR23C, ACTG1P1, 29 more genes
    nsv6299445copy number variation1nstd186human GRCh37 chr3: 137,849,491-137,936,590 , GRCh38.p12 chr3: 138,130,649-138,217,748 ARMC8, A4GNT, 1 more genes
    nsv6134785copy number variation1nstd213human GRCh37 chr3: 135,840,000-139,360,001 , GRCh38.p12 chr3: 136,121,158-139,641,159 ACTG1P1, FOXL2, 59 more genes
    nsv6134408copy number variation1nstd213human GRCh37 chr3: 137,810,000-137,880,001 , GRCh38.p12 chr3: 138,091,158-138,161,159 A4GNT, DBR1, 2 more genes
    nsv5898720copy number variation1nstd209human GRCh38 chr3: 138,159,773-138,161,872 , GRCh37.p13 chr3: 137,878,615-137,880,714 DBR1
    nsv5889866copy number variation1nstd209human GRCh38 chr3: 137,097,814-139,588,879 , GRCh37.p13 chr3: 136,816,656-139,307,721 , LOC105374127, 42 more genes
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