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Items: 1 to 20 of 188

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7040149inversion1nstd229human GRCh38 chr3: 137,187,995-138,131,845 , GRCh37.p13 chr3: 136,906,837-137,850,687 LINC01210, LOC105374127, 11 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
    nsv6737684copy number variation1nstd229human GRCh38 chr3: 138,120,007-138,124,097 , GRCh37.p13 chr3: 137,838,849-137,842,939 A4GNT
    nsv6736223copy number variation1nstd229human GRCh38 chr3: 138,127,560-138,128,250 , GRCh37.p13 chr3: 137,846,402-137,847,092 A4GNT
    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
    nsv6722937copy number variation1nstd229human GRCh38 chr3: 136,813,721-138,134,157 , GRCh37.p13 chr3: 136,532,563-137,852,999 LOC105374128, IL20RB-AS1, 17 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
    nsv6628450copy number variation1nstd224human GRCh37 chr3: 137,781,674-137,843,487 , GRCh38.p12 chr3: 138,062,832-138,124,645 A4GNT, KRT8P36, 1 more genes
    nsv6366209copy number variation1nstd223human GRCh38 chr3: 138,048,112-138,126,083 , GRCh37.p13 chr3: 137,766,954-137,844,925 DZIP1L, KRT8P36, 2 more genes
    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
    nsv6064447insertion1nstd212human GRCh38 chr3: 138,126,527-138,126,527 , GRCh37.p13 chr3: 137,845,369-137,845,369 A4GNT
    nsv5951603insertion1nstd209human GRCh38 chr3: 138,126,527-138,126,527 , GRCh37.p13 chr3: 137,845,369-137,845,369 A4GNT
    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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