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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
    nsv6932445copy number variation1nstd229human GRCh38 chr12: 31,990,622-32,001,577 , GRCh37.p13 chr12: 32,143,556-32,154,511 RESF1
    nsv6932283copy number variation1nstd229human GRCh38 chr12: 31,864,696-32,076,791 , GRCh37.p13 chr12: 32,017,630-32,229,725 RESF1, LINC02422, 4 more genes
    nsv6927126copy number variation1nstd229human GRCh38 chr12: 31,965,720-32,149,895 , GRCh37.p13 chr12: 32,118,654-32,302,829 RESF1, BICD1
    nsv6927109copy number variation1nstd229human GRCh38 chr12: 31,904,366-31,963,731 , GRCh37.p13 chr12: 32,057,300-32,116,665 RESF1, LOC105369725, 2 more genes
    nsv6926838copy number variation1nstd229human GRCh38 chr12: 31,990,746-31,996,895 , GRCh37.p13 chr12: 32,143,680-32,149,829 RESF1
    nsv6926181copy number variation1nstd229human GRCh38 chr12: 31,949,901-32,053,300 , GRCh37.p13 chr12: 32,102,835-32,206,234 LOC105369725, LOC100132543, 1 more genes
    nsv6922098copy number variation1nstd229human GRCh38 chr12: 31,981,301-32,092,300 , GRCh37.p13 chr12: 32,134,235-32,245,234 RESF1
    nsv6920003copy number variation1nstd229human GRCh38 chr12: 31,976,267-31,980,076 , GRCh37.p13 chr12: 32,129,201-32,133,010 RESF1
    nsv6919705copy number variation1nstd229human GRCh38 chr12: 31,854,501-32,142,800 , GRCh37.p13 chr12: 32,007,435-32,295,734 RESF1, RPLP2P4, 5 more genes
    nsv6918778copy number variation1nstd229human GRCh38 chr12: 31,992,848-31,998,264 , GRCh37.p13 chr12: 32,145,782-32,151,198 RESF1
    nsv6583285inversion1nstd223human GRCh38 chr12: 31,988,964-31,989,177 , GRCh37.p13 chr12: 32,141,898-32,142,111 RESF1
    nsv6583081inversion1nstd223human GRCh38 chr12: 31,976,690-31,977,371 , GRCh37.p13 chr12: 32,129,624-32,130,305 RESF1
    nsv6582976inversion1nstd223human GRCh38 chr12: 31,993,489-31,994,043 , GRCh37.p13 chr12: 32,146,423-32,146,977 RESF1
    nsv6474743copy number variation1nstd223human GRCh38 chr12: 31,956,701-31,959,400 , GRCh37.p13 chr12: 32,109,635-32,112,334 RESF1, LOC105369725
    nsv6456181copy number variation1nstd223human GRCh38 chr12: 31,976,265-31,980,075 , GRCh37.p13 chr12: 32,129,199-32,133,009 RESF1
    nsv6132243copy number variation1nstd213human GRCh37 chr12: 31,860,000-34,000,001 , GRCh38.p12 chr12: 31,707,066-33,847,066 ASS1P14, BICD1, 26 more genes
    nsv6132242copy number variation1nstd213human GRCh37 chr12: 31,860,000-32,630,001 , GRCh38.p12 chr12: 31,707,066-32,477,067 BICD1, AMN1, 16 more genes
    nsv6132241copy number variation1nstd213human GRCh37 chr12: 31,410,000-34,000,001 , GRCh38.p12 chr12: 31,257,066-33,847,066 ASS1P14, BICD1, 39 more genes
    nsv5971298inversion1nstd209human GRCh38 chr12: 31,979,101-31,989,231 , GRCh37.p13 chr12: 32,132,035-32,142,165 RESF1
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