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Items: 1 to 20 of 175

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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
    nsv7064476inversion1nstd229human GRCh38 chr11: 123,462,060-125,907,500 , GRCh37.p13 chr11: 123,332,768-125,777,395 STT3A, OR8G1, 101 more genes
    nsv6916629copy number variation1nstd229human GRCh38 chr11: 124,677,241-124,788,089 , GRCh37.p13 chr11: 124,547,137-124,657,985 ESAM, VSIG2, 5 more genes
    nsv6916077copy number variation1nstd229human GRCh38 chr11: 124,575,701-124,974,400 , GRCh37.p13 chr11: 124,445,597-124,844,296 SIAE, HEPACAM, 19 more genes
    nsv6904525copy number variation1nstd229human GRCh38 chr11: 124,765,979-124,766,030 , GRCh37.p13 chr11: 124,635,875-124,635,926 ESAM-AS1, MSANTD2
    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
    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
    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
    nsv6206720copy number variation1nstd214human GRCh38 chr11: 124,765,979-124,766,029 , GRCh37.p13 chr11: 124,635,875-124,635,925 MSANTD2, ESAM-AS1
    nsv6028150copy number variation1nstd212human GRCh38 chr11: 124,765,979-124,766,030 , GRCh37.p13 chr11: 124,635,875-124,635,926 ESAM-AS1, MSANTD2
    nsv5925923copy number variation1nstd209human GRCh38 chr11: 124,765,979-124,766,029 , GRCh37.p13 chr11: 124,635,875-124,635,925 ESAM-AS1, MSANTD2
    nsv5501725copy number variation1nstd206human GRCh38 chr11: 124,765,979-124,766,030 , GRCh37.p13 chr11: 124,635,875-124,635,926 MSANTD2, ESAM-AS1
    nsv4981133copy number variation1nstd200human GRCh38 chr11: 124,765,362-124,766,575 , GRCh37.p13 chr11: 124,635,258-124,636,471 MSANTD2, ESAM-AS1
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 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
    nsv4674572copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571 ACRV1, APLP2, 382 more genes
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