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Items: 1 to 20 of 190

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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
    nsv7077728inversion1nstd229human GRCh38 chr11: 124,239,803-134,089,458 , GRCh37.p13 chr11: 124,110,545-133,959,353 LOC283172, PPP1R10P1, 175 more genes
    nsv7070443inversion1nstd229human GRCh38 chr11: 125,887,512-126,792,902 , GRCh37.p13 chr11: 125,757,407-126,662,797 CDON, TIRAP, 21 more genes
    nsv6907021copy number variation1nstd229human GRCh38 chr11: 125,951,086-125,953,359 , GRCh37.p13 chr11: 125,820,981-125,823,254 VSIG10L2
    nsv6906616copy number variation1nstd229human GRCh38 chr11: 125,953,511-125,972,187 , GRCh37.p13 chr11: 125,823,406-125,842,082 VSIG10L2, CDON
    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
    nsv6637236copy number variation1nstd102humanUncertain significance GRCh37 chr11: 125,812,020-126,308,722 , GRCh38.p12 chr11: 125,942,125-126,438,827 RPL35AP26, RNU4-86P, 16 more genes
    nsv6473263copy number variation1nstd223human GRCh38 chr11: 125,907,418-125,971,152 , GRCh37.p13 chr11: 125,777,313-125,841,047 CDON, DDX25, 1 more genes
    nsv6468167copy number variation1nstd223human GRCh38 chr11: 125,951,086-125,953,352 , GRCh37.p13 chr11: 125,820,981-125,823,247 VSIG10L2
    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
    nsv6309036copy number variation3nstd102humanUncertain significance GRCh37 chr11: 123,504,851-126,163,012 , GRCh38.p12 chr11: 123,634,143-126,293,117 CDON, PKNOX2-DT, 113 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
    nsv6291035copy number variation1nstd102humanUncertain significance GRCh37 chr11: 125,569,544-125,939,872 , GRCh38.p12 chr11: 125,699,649-126,069,977 CDON, PATE1, 9 more genes
    nsv6291027copy number variation1nstd102humanUncertain significance GRCh37 chr11: 125,778,528-125,836,238 , GRCh38.p12 chr11: 125,908,633-125,966,343 VSIG10L2, DDX25, 1 more genes
    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
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4729126copy number variation1nstd102humanUncertain significance GRCh37 chr11: 125,777,055-125,838,856 , GRCh38.p12 chr11: 125,907,160-125,968,961 CDON, DDX25, 1 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
    nsv4675674copy number variation1nstd102humanPathogenic GRCh37 chr11: 124,232,608-134,938,470 , GRCh38.p12 chr11: 124,362,712-135,068,576 FAM118B, PUS3, 184 more genes
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