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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093915copy number variation1nstd102humanPathogenic GRCh37 chr11: 111,171,709-111,958,707 , GRCh38.p12 chr11: 111,300,984-112,087,983 CRYAB, BTG4, 34 more genes
    nsv7093832copy number variation1nstd102humanUncertain significance GRCh37 chr11: 111,957,547-111,959,745 , GRCh38.p12 chr11: 112,086,823-112,089,021 TIMM8B, SDHD
    nsv7093830copy number variation1nstd102humanPathogenic GRCh37 chr11: 111,171,709-111,959,745 , GRCh38.p12 chr11: 111,300,984-112,089,021 LOC100132078, DLAT, 34 more genes
    nsv7093669copy number variation2nstd102humanUncertain significance GRCh37 chr11: 111,171,709-112,104,278 , GRCh38.p12 chr11: 111,300,984-112,233,555 CRYAB, RPS6P16, 43 more genes
    nsv7074145inversion1nstd229human GRCh38 chr11: 104,112,094-113,544,164 , GRCh37.p13 chr11: 103,982,822-113,414,886 COLCA1, LOC105369491, 150 more genes
    nsv7069281inversion1nstd229human GRCh38 chr11: 107,936,485-114,400,629 , GRCh37.p13 chr11: 107,807,211-114,271,351 LRRC37A13P, POU2AF3, 121 more genes
    nsv7065935inversion1nstd229human GRCh38 chr11: 107,044,115-113,544,291 , GRCh37.p13 chr11: 106,914,841-113,415,013 LINC02762, TIMM8B, 112 more genes
    nsv6916344copy number variation1nstd229human GRCh38 chr11: 111,909,401-112,149,800 , GRCh37.p13 chr11: 111,780,125-111,945,380 , GRCh37.p13 chr11|NW_003871080.1: 161,392-326,647 SDHD, TIMM8B, 12 more genes
    nsv6637811copy number variation1nstd102humanPathogenic GRCh37 chr11: 109,328,787-116,414,966 , GRCh38.p12 chr11: 109,458,061-116,544,249 LOC102723966, NXPE4, 129 more genes
    nsv6620695copy number variation1nstd224human GRCh37 chr11: 111,953,288-112,208,967 , GRCh38.p12 chr11: 112,082,564-112,338,244 TIMM8B, NKAPD1, 15 more genes
    nsv6586218inversion1nstd223human GRCh38 chr11: 107,936,497-114,408,912 , GRCh37.p13 chr11: 107,807,223-114,279,634 LOC107984390, ATF4P4, 121 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
    nsv6308961copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr11: 111,957,632-111,965,694 , GRCh38.p12 chr11: 112,086,908-112,094,970 SDHD, TIMM8B
    nsv6308959copy number variation1nstd102humanUncertain significance GRCh37 chr11: 111,779,478-111,961,866 , GRCh38.p12 chr11: 111,908,754-112,091,142 HSPB2, PIH1D2, 11 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
    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
    nsv6112674copy number variation1nstd102humanPathogenic GRCh37 chr11: 111,957,571-111,966,518 , GRCh38.p12 chr11: 112,086,847-112,095,794 SDHD, TIMM8B
    nsv6032625copy number variation1nstd212human GRCh37.p13 chr11: 111,947,896-112,052,189 , GRCh38 chr11: 112,077,172-112,181,466 IL18, SDHD, 6 more genes
    nsv5708427mobile element insertion2nstd211human GRCh38 chr11: 112,084,386-112,084,386 , GRCh37.p13 chr11: 111,955,110-111,955,110 TIMM8B, NKAPD1
    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
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