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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7061170inversion1nstd229human GRCh38 chr11: 96,321,682-96,403,554 , GRCh37.p13 chr11: 96,054,846-96,136,718 MAML2, MIR1260B, 2 more genes
    nsv7060154inversion1nstd229human GRCh38 chr11: 89,626,991-96,425,689 , GRCh37.p13 chr11: 89,360,159-96,158,853 LINC02756, OSBPL9P2, 119 more genes
    nsv6916067copy number variation1nstd229human GRCh38 chr11: 96,086,687-98,006,306 , GRCh37.p13 chr11: 95,819,851-97,877,034 JRKL-AS1, LINC02713, 14 more genes
    nsv6912952copy number variation1nstd229human GRCh38 chr11: 96,385,418-96,390,206 , GRCh37.p13 chr11: 96,118,582-96,123,370 CCDC82, JRKL
    nsv6907347copy number variation1nstd229human GRCh38 chr11: 89,715,432-96,566,090 , GRCh37.p13 chr11: 89,448,600-96,287,584 DISC1FP1, RPL32P25, 120 more genes
    nsv6904725copy number variation1nstd229human GRCh38 chr11: 96,272,974-100,539,553 , GRCh37.p13 chr11: 96,006,138-100,410,284 RN7SKP53, RPA2P3, 22 more genes
    nsv6904034copy number variation1nstd229human GRCh38 chr11: 96,391,617-96,391,832 , GRCh37.p13 chr11: 96,124,781-96,124,996 JRKL
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 LOC107984375, RN7SL222P, 295 more genes
    nsv6582429inversion1nstd223human GRCh38 chr11: 93,899,951-96,855,215 , GRCh37.p13 chr11: 93,633,117-96,726,215 MIR1260B, KDM4E, 51 more genes
    nsv6469262copy number variation1nstd223human GRCh38 chr11: 96,086,687-98,006,306 , GRCh37.p13 chr11: 95,819,851-97,877,034 LOC105369450, LOC105369453, 14 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6313961copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,855,209-98,002,445 , GRCh38.p12 chr11: 78,144,163-98,131,717 MTND5P38, XIAPP2, 252 more genes
    nsv6290834copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956 CARD17P, RNA5SP350, 480 more genes
    nsv6132294copy number variation1nstd213human GRCh37 chr11: 95,460,000-96,160,001 , GRCh38.p12 chr11: 95,726,836-96,426,837 RNA5SP345, RPL32P25, 8 more genes
    nsv6132125copy number variation1nstd213human GRCh37 chr11: 95,800,000-96,210,001 , GRCh38.p12 chr11: 96,066,836-96,476,837 JRKL, CCDC82, 4 more genes
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5037979inversion1nstd200human GRCh38 chr11: 93,899,952-96,855,215 , GRCh37.p13 chr11: 93,633,118-96,726,215 , GPR83, 52 more genes
    nsv4989189copy number variation1nstd200human GRCh38 chr11: 96,253,825-96,817,793 , GRCh37.p13 chr11: 95,986,989-96,688,793 MIR1260B, RNA5SP346, 6 more genes
    nsv4728836copy number variation1nstd102humanUncertain significance GRCh37 chr11: 95,822,513-97,875,558 , GRCh38.p12 chr11: 96,089,349-98,004,830 CCDC82, RNA5SP347, 14 more genes
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