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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143805copy number variation1nstd232human GRCh37.p13 chr11: 57,509,188-57,509,278 , GRCh38.p12 chr11: 57,741,716-57,741,806 SELENOH, BTBD18, 1 more genes
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv6464947copy number variation1nstd223human GRCh38 chr11: 57,741,401-57,741,900 , GRCh37.p13 chr11: 57,508,873-57,509,372 BTBD18, SELENOH, 2 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
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv6291401copy number variation1nstd102humannot provided GRCh37 chr11: 57,112,299-57,871,866 , GRCh38.p12 chr11: 57,344,825-58,104,394 RN7SL605P, CLP1, 35 more genes
    nsv6101017inversion1nstd212human GRCh38 chr11: 54,578,670-59,501,927 , GRCh37.p13 chr11: 54,711,406-59,269,400 , APLNR, 236 more genes
    nsv5914325copy number variation1nstd209human GRCh38 chr11: 55,273,256-58,053,631 , GRCh37.p13 chr11: 55,040,732-57,821,103 , LOC107984365, 161 more genes
    nsv5672633copy number variation1nstd102humanPathogenic GRCh37 chr11: 57,471,510-57,564,464 , GRCh38.p12 chr11: 57,704,038-57,796,992 CTNND1, TMX2, 5 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
    nsv5355205translocation1nstd200human GRCh38 chr11: 57,742,247-57,742,247 , GRCh38 chr11: 57,742,860-57,742,860 , GRCh37.p13 chr11: 57,510,332-57,510,332 , GRCh37.p13 chr11: 57,509,719-57,509,719 SELENOH, BTBD18, 1 more genes
    nsv5355204translocation1nstd200human GRCh38 chr11: 57,742,116-57,742,116 , GRCh38 chr11: 57,741,956-57,741,956 , GRCh37.p13 chr11: 57,509,428-57,509,428 , GRCh37.p13 chr11: 57,509,588-57,509,588 SELENOH, BTBD18, 1 more genes
    nsv5355203translocation1nstd200human GRCh38 chr11: 57,741,807-57,741,807 , GRCh38 chr11: 57,741,717-57,741,717 , GRCh37.p13 chr11: 57,509,279-57,509,279 , GRCh37.p13 chr11: 57,509,189-57,509,189 SELENOH, BTBD18, 1 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4527727copy number variation1nstd166human GRCh37.p13 chr11: 57,509,428-57,510,332 , GRCh38.p12 chr11: 57,741,956-57,742,860 SELENOH, BTBD18, 1 more genes
    nsv4453292copy number variation1nstd102humannot provided GRCh37 chr11: 55,033,164-57,518,726 , GRCh38.p12 chr11: 55,265,688-57,751,254 OR8J3, LINC02735, 150 more genes
    nsv4202685copy number variation1nstd166human GRCh37.p13 chr11: 57,509,428-57,509,588 , GRCh38.p12 chr11: 57,741,956-57,742,116 BTBD18, TMX2-CTNND1, 1 more genes
    nsv4200217copy number variation1nstd166human GRCh37.p13 chr11: 57,509,189-57,509,279 , GRCh38.p12 chr11: 57,741,717-57,741,807 BTBD18, TMX2-CTNND1, 1 more genes
    nsv3918477copy number variation1nstd102humanUncertain significance GRCh38 chr11: 57,372,226-57,936,167 , NCBI36 chr11: 56,896,275-57,460,215 , GRCh37 chr11: 57,139,699-57,703,639 TMX2-CTNND1, CTNND1, 26 more genes
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