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Items: 1 to 20 of 223

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137129copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659 VSIG10L2, OR8B6P, 268 more genes
    nsv7093673copy number variation1nstd102humanUncertain significance GRCh37 chr11: 128,564,154-128,786,626 , GRCh38.p12 chr11: 128,694,259-128,916,731 FLI1, KCNJ1, 4 more genes
    nsv7077728inversion1nstd229human GRCh38 chr11: 124,239,803-134,089,458 , GRCh37.p13 chr11: 124,110,545-133,959,353 LOC283172, PPP1R10P1, 175 more genes
    nsv7069138inversion1nstd229human GRCh38 chr11: 128,470,446-128,811,017 , GRCh37.p13 chr11: 128,340,341-128,680,912 SENCR, LOC101929538, 6 more genes
    nsv6912205copy number variation1nstd229human GRCh38 chr11: 128,538,001-129,014,800 , GRCh37.p13 chr11: 128,407,896-128,884,695 KCNJ1, KCNJ5-AS1, 11 more genes
    nsv6899526copy number variation1nstd229human GRCh38 chr11: 128,694,428-128,695,090 , GRCh37.p13 chr11: 128,564,323-128,564,985 FLI1, SENCR
    nsv6637558copy number variation1nstd102humanPathogenic GRCh37 chr11: 122,975,824-134,938,470 , GRCh38.p12 chr11: 123,105,116-135,068,576 OR8B8, LOC107984373, 234 more genes
    nsv6634467copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 127,074,235-135,006,516 , GRCh38.p12 chr11: 127,204,340-135,076,622 APLP2, BAK1P2, 98 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
    nsv6291074copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847 ZW10, MPZL2, 378 more genes
    nsv6290152copy number variation1nstd102humanPathogenic GRCh37 chr11: 128,561,665-128,682,728 , GRCh38.p12 chr11: 128,691,770-128,812,833 FLI1, SENCR
    nsv6289927copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522 IGSF9B, MIR10526, 592 more genes
    nsv6132083copy number variation1nstd213human GRCh37 chr11: 126,840,000-128,920,001 , GRCh38.p12 chr11: 126,970,104-129,050,106 ETS1, KCNJ1, 28 more genes
    nsv5662720insertion1nstd207human GRCh38 chr11: 128,695,049-128,695,049 , GRCh37.p13 chr11: 128,564,944-128,564,944 FLI1, SENCR
    nsv5341011translocation1nstd200human GRCh37 chr11: 128,564,932-128,564,932 , GRCh37 chr11: 128,564,850-128,564,850 , GRCh38.p12 chr11: 128,695,037-128,695,037 , GRCh38.p12 chr11: 128,694,955-128,694,955 FLI1, SENCR
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4729012copy number variation1nstd102humanPathogenic GRCh37 chr11: 127,602,115-134,938,470 , GRCh38.p12 chr11: 127,732,220-135,068,576 LINC02706, APLP2, 92 more genes
    nsv4728891copy number variation1nstd102humanPathogenic GRCh37 chr11: 125,785,487-134,938,470 , GRCh38.p12 chr11: 125,915,592-135,068,576 ARHGAP32, NAP1L1P1, 125 more genes
    nsv4675832copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,742,540-134,938,470 , GRCh38.p12 chr11: 120,871,831-135,068,576 MIR8052, BLID, 275 more genes
    nsv4675703copy number variation1nstd102humanUncertain significance GRCh37 chr11: 128,194,490-128,595,064 , GRCh38.p12 chr11: 128,324,595-128,725,169 FLI1, SENCR, 6 more genes
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