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Items: 1 to 20 of 93

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093695copy number variation1nstd102humanUncertain significance GRCh37 chr11: 61,731,556-61,735,061 , GRCh38.p12 chr11: 61,964,084-61,967,589 LOC399900, FTH1, 1 more genes
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv7077001inversion1nstd229human GRCh38 chr11: 61,961,332-62,482,821 , GRCh37.p13 chr11: 61,728,804-62,250,293 SCGB2A1, INCENP, 16 more genes
    nsv7076799inversion1nstd229human GRCh38 chr11: 61,964,679-61,964,848 , GRCh37.p13 chr11: 61,732,151-61,732,320 BEST1, FTH1
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv6917433copy number variation1nstd229human GRCh38 chr11: 61,472,401-62,010,600 , GRCh37.p13 chr11: 61,239,873-61,778,072 LOC105369329, FADS3, 24 more genes
    nsv6916562copy number variation1nstd229human GRCh38 chr11: 61,877,316-62,000,326 , GRCh37.p13 chr11: 61,644,788-61,767,798 RNU6-1243P, BEST1, 6 more genes
    nsv6912130copy number variation1nstd229human GRCh38 chr11: 61,964,109-61,966,360 , GRCh37.p13 chr11: 61,731,581-61,733,832 BEST1, LOC399900, 1 more genes
    nsv6909200copy number variation1nstd229human GRCh38 chr11: 61,458,001-62,069,400 , GRCh37.p13 chr11: 61,225,473-61,836,872 RPS2P37, BEST1, 25 more genes
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6904042copy number variation1nstd229human GRCh38 chr11: 61,456,701-62,012,000 , GRCh37.p13 chr11: 61,224,173-61,779,472 LOC399900, LRRC10B, 24 more genes
    nsv6903235copy number variation1nstd229human GRCh38 chr11: 61,951,453-61,962,421 , GRCh37.p13 chr11: 61,718,925-61,729,893 LOC107984334, FTH1, 1 more genes
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 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
    nsv6309224copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 61,725,598-61,730,385 , GRCh38.p12 chr11: 61,958,126-61,962,913 FTH1, BEST1, 1 more genes
    nsv5672536copy number variation1nstd102humanPathogenic GRCh37 chr11: 61,729,938-61,730,007 , GRCh38 chr11: 61,962,466-61,962,535 FTH1, BEST1
    nsv5380804copy number variation1nstd102humanUncertain significance GRCh37 chr11: 61,731,556-61,732,604 , GRCh38.p12 chr11: 61,964,084-61,965,132 FTH1, BEST1
    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
    nsv5276562copy number variation1nstd204human GRCh38.p13 chr11: 61,954,301-61,982,800 , GRCh37.p13 chr11: 61,721,773-61,750,272 LOC107984334, BEST1, 2 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
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