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Items: 1 to 20 of 81

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv7068318inversion1nstd229human GRCh38 chr11: 58,150,576-58,242,317 , GRCh37.p13 chr11: 57,918,048-58,009,789 OR5BL1P, OR9Q2, 5 more genes
    nsv6902872copy number variation1nstd229human GRCh38 chr11: 58,208,287-58,213,894 , GRCh37.p13 chr11: 57,975,759-57,981,366 OR1S1
    nsv6581122inversion1nstd223human GRCh38 chr11: 58,205,933-58,213,148 , GRCh37.p13 chr11: 57,973,405-57,980,620 OR1S1
    nsv6471354copy number variation1nstd223human GRCh38 chr11: 58,212,301-58,213,500 , GRCh37.p13 chr11: 57,979,773-57,980,972 OR1S1
    nsv6456650copy number variation1nstd223human GRCh38 chr11: 58,208,287-58,213,888 , GRCh37.p13 chr11: 57,975,759-57,981,360 OR1S1
    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
    nsv6101017inversion1nstd212human GRCh38 chr11: 54,578,670-59,501,927 , GRCh37.p13 chr11: 54,711,406-59,269,400 , APLNR, 236 more genes
    nsv5978690inversion1nstd209human GRCh38 chr11: 58,000,184-58,217,938 , GRCh37.p13 chr11: 57,767,656-57,985,410 OR9L1P, OR9I3P, 13 more genes
    nsv5559405inversion1nstd206human GRCh38 chr11: 58,205,830-58,213,132 , GRCh37.p13 chr11: 57,973,302-57,980,604 OR1S1
    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
    nsv4979533copy number variation1nstd200human GRCh38 chr11: 58,208,287-58,213,888 , GRCh37.p13 chr11: 57,975,759-57,981,360 OR1S1
    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
    nsv4418717copy number variation1nstd174human GRCh37 chr11: 57,967,767-57,983,112 , GRCh38.p12 chr11: 58,200,295-58,215,640 OR1S2, OR1S1
    nsv4334316sequence alteration1nstd166human GRCh37.p13 chr11: 57,918,047-58,133,767 , GRCh38.p12 chr11: 58,150,575-58,366,294 OR9Q2, OR10Q1, 13 more genes
    nsv4206126copy number variation1nstd166human GRCh37.p13 chr11: 57,972,482-57,981,674 , GRCh38.p12 chr11: 58,205,010-58,214,202 OR1S1
    nsv3969455insertion1nstd168human GRCh38 chr11: 58,215,281-58,223,829 , GRCh37.p13 chr11: 57,982,753-57,991,301 OR1S1
    nsv3911150copy number variation1nstd102humanPathogenic GRCh37 chr11: 55,086,995-58,766,250 , NCBI36 chr11: 54,843,571-58,522,826 , GRCh38 chr11: 55,319,519-58,998,777 OR5BD1P, SELENOH, 197 more genes
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