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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7060154inversion1nstd229human GRCh38 chr11: 89,626,991-96,425,689 , GRCh37.p13 chr11: 89,360,159-96,158,853 LINC02756, OSBPL9P2, 119 more genes
    nsv6917390copy number variation1nstd229human GRCh38 chr11: 95,068,075-95,071,767 , GRCh37.p13 chr11|NW_003871079.1: 189,395-193,088 , GRCh37.p13 chr11: 94,801,238-94,804,931 SRSF8
    nsv6914514copy number variation1nstd229human GRCh38 chr11: 95,059,980-95,165,673 , GRCh37.p13 chr11: 94,793,144-94,852,618 , GRCh37.p13 chr11|NW_003871079.1: 181,300-240,775 ENDOD1, LNCRNA-IUR, 3 more genes
    nsv6912565copy number variation1nstd229human GRCh38 chr11: 95,068,461-95,144,521 , GRCh37.p13 chr11|NW_003871079.1: 189,781-240,775 , GRCh37.p13 chr11: 94,801,624-94,852,618 ENDOD1, SRSF8, 1 more genes
    nsv6907347copy number variation1nstd229human GRCh38 chr11: 89,715,432-96,566,090 , GRCh37.p13 chr11: 89,448,600-96,287,584 DISC1FP1, RPL32P25, 120 more genes
    nsv6900323copy number variation1nstd229human GRCh38 chr11: 93,200,748-96,340,159 , GRCh37.p13 chr11: 92,933,914-96,073,323 FGFR3P2, LOC112268080, 67 more genes
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 LOC107984375, RN7SL222P, 295 more genes
    nsv6634412copy number variation1nstd102humanUncertain significance GRCh37 chr11: 94,693,565-95,725,474 , GRCh38.p12 chr11: 94,960,400-95,992,310 SRSF8, LOC105369439, 25 more genes
    nsv6582429inversion1nstd223human GRCh38 chr11: 93,899,951-96,855,215 , GRCh37.p13 chr11: 93,633,117-96,726,215 MIR1260B, KDM4E, 51 more genes
    nsv6468916copy number variation1nstd223human GRCh38 chr11: 95,064,501-95,070,700 , GRCh37.p13 chr11: 94,797,665-94,803,863 , GRCh37.p13 chr11|NW_003871079.1: 185,821-192,020 SRSF8
    nsv6461824copy number variation1nstd223human GRCh38 chr11: 95,059,101-95,096,500 , GRCh37.p13 chr11: 94,792,265-94,829,664 , GRCh37.p13 chr11|NW_003871079.1: 180,421-217,821 ENDOD1, SRSF8
    nsv6459070copy number variation1nstd223human GRCh38 chr11: 92,156,862-95,481,795 , GRCh37.p13 chr11: 91,890,028-95,214,959 FUT4, KDM4D, 66 more genes
    nsv6456993copy number variation1nstd223human GRCh38 chr11: 95,066,301-95,072,000 , GRCh37.p13 chr11|NW_003871079.1: 187,621-193,321 , GRCh37.p13 chr11: 94,799,465-94,805,164 SRSF8
    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
    nsv6313961copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,855,209-98,002,445 , GRCh38.p12 chr11: 78,144,163-98,131,717 MTND5P38, XIAPP2, 252 more genes
    nsv6291243copy number variation1nstd102humanUncertain significance GRCh37 chr11: 94,681,351-95,176,293 , GRCh38.p12 chr11: 94,948,186-95,443,129 LOC100129203, LOC100420801, 14 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
    nsv5976640insertion1nstd209human GRCh38 chr11: 95,070,368-95,070,368 , GRCh37.p13 chr11: 94,803,531-94,803,531 , GRCh37.p13 chr11|NW_003871079.1: 191,688-191,688 SRSF8
    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
    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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