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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070460inversion1nstd229human GRCh38 chr11: 21,520,035-27,618,155 , GRCh37.p13 chr11: 21,541,581-27,639,702 RPS25P1, LOC105376598, 48 more genes
    nsv7068221inversion1nstd229human GRCh38 chr11: 22,389,577-22,666,119 , GRCh37.p13 chr11: 22,411,123-22,687,665 LINC01495, LOC105376588, 2 more genes
    nsv7068073inversion1nstd229human GRCh38 chr11: 22,521,553-22,761,203 , GRCh37.p13 chr11: 22,543,099-22,782,749 FANCF, RNA5SP338, 1 more genes
    nsv7067025inversion1nstd229human GRCh38 chr11: 22,307,930-23,197,158 , GRCh37.p13 chr11: 22,329,476-23,218,704 SLC17A6, FANCF, 7 more genes
    nsv7064543inversion1nstd229human GRCh38 chr11: 22,291,416-22,707,330 , GRCh37.p13 chr11: 22,312,962-22,728,876 GAS2, LINC01495, 4 more genes
    nsv7058561inversion1nstd229human GRCh38 chr11: 22,022,654-22,865,606 , GRCh37.p13 chr11: 22,044,200-22,887,152 CCDC179, GAS2, 8 more genes
    nsv6914519copy number variation1nstd229human GRCh38 chr11: 22,603,937-22,620,895 , GRCh37.p13 chr11: 22,625,483-22,642,441 FANCF
    nsv6913291copy number variation1nstd229human GRCh38 chr11: 22,578,310-22,674,904 , GRCh37.p13 chr11: 22,599,856-22,696,450 FANCF, GAS2
    nsv6906158copy number variation1nstd229human GRCh38 chr11: 18,831,701-26,837,040 , GRCh37.p13 chr11: 18,853,248-26,858,587 HTATIP2, LINC02686, 68 more genes
    nsv6901911copy number variation1nstd229human GRCh38 chr11: 22,259,617-22,699,628 , GRCh37.p13 chr11: 22,281,163-22,721,174 ANO5, LINC01495, 5 more genes
    nsv6637345copy number variation1nstd102humanUncertain significance GRCh37 chr11: 22,582,555-23,040,011 , GRCh38.p12 chr11: 22,561,009-23,018,465 SVIP, GAS2, 3 more genes
    nsv6637344copy number variation1nstd102humanUncertain significance GRCh37 chr11: 22,501,365-22,701,807 , GRCh38.p12 chr11: 22,479,819-22,680,261 FANCF, GAS2, 2 more genes
    nsv6437352copy number variation1nstd223human GRCh38 chr11: 22,603,937-22,620,891 , GRCh37.p13 chr11: 22,625,483-22,642,437 FANCF
    nsv6437088copy number variation1nstd223human GRCh38 chr11: 22,625,767-22,648,931 , GRCh37.p13 chr11: 22,647,313-22,670,477 GAS2, FANCF
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6314682copy number variation1nstd102humanPathogenic GRCh37 chr11: 22,644,078-22,647,388 , GRCh38.p12 chr11: 22,622,532-22,625,842 GAS2, FANCF
    nsv6313990copy number variation1nstd102humanUncertain significance GRCh37 chr11: 22,469,479-22,724,326 , GRCh38.p12 chr11: 22,447,933-22,702,780 LOC105376588, RNA5SP338, 3 more genes
    nsv6309192copy number variation1nstd102humanUncertain significance GRCh37 chr11: 22,646,232-22,647,356 , GRCh38.p12 chr11: 22,624,686-22,625,810 FANCF, GAS2
    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
    nsv5380723copy number variation1nstd102humanUncertain significance GRCh37 chr11: 22,646,226-22,647,362 , GRCh38.p12 chr11: 22,624,680-22,625,816 FANCF, GAS2
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