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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5916755copy number variation1nstd209human GRCh38 chr11: 46,307,212-46,307,353 , GRCh37.p13 chr11: 46,328,763-46,328,904 CREB3L1
    nsv5915076copy number variation1nstd209human GRCh38 chr11: 46,314,188-46,314,277 , GRCh37.p13 chr11: 46,335,739-46,335,828 CREB3L1
    nsv5914622copy number variation1nstd209human GRCh38 chr11: 46,303,407-46,303,762 , GRCh37.p13 chr11: 46,324,958-46,325,313 CREB3L1
    nsv5696871mobile element insertion1nstd211human GRCh38 chr11: 46,296,475-46,296,475 , GRCh37.p13 chr11: 46,318,026-46,318,026 CREB3L1
    nsv5546297insertion1nstd206human GRCh38 chr11: 46,282,412-46,282,412 , GRCh37.p13 chr11: 46,303,963-46,303,963 CREB3L1
    nsv5503655copy number variation1nstd206human GRCh38 chr11: 46,276,833-46,276,895 , GRCh37.p13 chr11: 46,298,384-46,298,446 CREB3L1
    nsv5501156copy number variation1nstd206human GRCh38 chr11: 46,180,818-46,311,485 , GRCh37.p13 chr11: 46,202,369-46,333,036 CREB3L1, LINC02489, 1 more genes
    nsv5409494mobile element insertion1nstd206human GRCh38 chr11: 46,296,475-46,296,526 , GRCh37.p13 chr11: 46,318,026-46,318,077 CREB3L1
    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
    nsv5380725copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 45,827,353-47,804,770 , GRCh38.p12 chr11: 45,805,802-47,783,218 MIR4688, LOC112268075, 58 more genes
    nsv5125160mobile element insertion1nstd203human GRCh38 chr11: 46,296,460-46,296,475 , GRCh37.p13 chr11: 46,318,011-46,318,026 CREB3L1
    nsv4841073copy number variation1nstd200human GRCh37 chr11: 46,328,763-46,328,915 , GRCh38.p12 chr11: 46,307,212-46,307,364 CREB3L1
    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
    nsv4729454copy number variation1nstd102humanUncertain significance GRCh37 chr11: 46,123,974-46,442,526 , GRCh38.p12 chr11: 46,102,423-46,420,976 CHRM4, MDK, 10 more genes
    nsv4729122copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 45,995,260-46,536,343 , GRCh38.p12 chr11: 45,973,709-46,514,793 CHRM4, MDK, 13 more genes
    nsv4577964mobile element insertion1nstd166human GRCh37.p13 chr11: 46,339,687-46,339,687 , GRCh38.p12 chr11: 46,318,136-46,318,136 CREB3L1
    nsv4568416sequence alteration1nstd166human GRCh37.p13 chr11: 46,303,962-46,305,147 , GRCh38.p12 chr11: 46,282,411-46,283,596 CREB3L1
    nsv4456633copy number variation1nstd102humanUncertain significance GRCh37 chr11: 46,302,171-46,783,079 , GRCh38.p12 chr11: 46,280,620-46,761,529 MIR5582, RPS10P19, 15 more genes
    nsv4389820copy number variation1nstd171human GRCh37 chr11: 46,319,023-46,319,060 , GRCh38.p12 chr11: 46,297,472-46,297,509 CREB3L1
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