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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098704complex chromosomal rearrangement5nstd230human GRCh37 chr5: 2,891,584-2,891,584 , GRCh37 chr5: 2,891,590-2,891,590 , GRCh37 chr5: 27,729,445-27,729,445 , GRCh37 chr5: 27,729,449-27,729,449 , GRCh37 chr7: 117,155,534-117,155,534 , GRCh37 chr7: 117,155,535-117,155,535 , GRCh37 chr11: 111,447,337-111,447,337 , GRCh37 chr11: 111,447,920-111,447,920 , GRCh37 chr11: 111,795,048-111,795,048 , GRCh37 chr11: 111,795,273-111,795,273 , GRCh38.p12 chr11: 111,576,612-111,576,612 , GRCh38.p12 chr11: 111,577,195-111,577,195 , GRCh38.p12 chr11: 111,924,324-111,924,324 , GRCh38.p12 chr11: 111,924,549-111,924,549 , GRCh38.p12 chr5: 2,891,470-2,891,470 , GRCh38.p12 chr5: 2,891,476-2,891,476 , GRCh38.p12 chr5: 27,729,338-27,729,338 , GRCh38.p12 chr5: 27,729,342-27,729,342 , GRCh38.p12 chr7: 117,515,480-117,515,480 , GRCh38.p12 chr7: 117,515,481-117,515,481 CFTR, C11orf52, 1 more genes
    nsv7093916copy number variation1nstd102humanPathogenic GRCh37 chr11: 111,657,121-111,922,093 , GRCh38.p12 chr11: 111,786,397-112,051,369 RPL37AP8, DIXDC1, 13 more genes
    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
    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
    nsv6898629copy number variation1nstd229human GRCh38 chr11: 111,807,347-111,971,481 , GRCh37.p13 chr11: 111,678,071-111,842,205 , GRCh37.p13 chr11|NW_003871080.1: 59,339-223,472 RNA5SP351, HSPB2, 9 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
    nsv6620949copy number variation1nstd224human GRCh37 chr11: 111,608,216-111,856,033 , GRCh38.p12 chr11: 111,737,492-111,985,309 PPP2R1B, DIXDC1, 10 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
    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
    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
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 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
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