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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147644insertion1nstd232human GRCh37.p13 chr11: 60,666,777-60,666,777 , GRCh38.p12 chr11: 60,899,305-60,899,305 PRPF19
    nsv7144106insertion1nstd232human GRCh37.p13 chr11: 60,658,738-60,658,738 , GRCh38.p12 chr11: 60,891,266-60,891,266 PRPF19
    nsv7142580insertion1nstd232human GRCh37.p13 chr11: 60,665,748-60,665,748 , GRCh38.p12 chr11: 60,898,276-60,898,276 PRPF19
    nsv7138014insertion1nstd232human GRCh37.p13 chr11: 60,670,354-60,670,354 , GRCh38.p12 chr11: 60,902,882-60,902,882 PRPF19
    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
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 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
    nsv6903566copy number variation1nstd229human GRCh38 chr11: 60,888,283-60,933,862 , GRCh37.p13 chr11: 60,655,756-60,701,334 PRPF19, TMEM109, 3 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
    nsv6462052copy number variation1nstd223human GRCh38 chr11: 60,885,041-60,889,479 , GRCh37.p13 chr11: 60,652,514-60,656,952 PRPF19
    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
    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
    nsv5325627inversion1nstd204human GRCh37.p13 chr11: 58,669,453-61,321,541 , GRCh38.p13 chr11: 58,901,980-61,554,069 , CD5, 118 more genes
    nsv5183330mobile element insertion1nstd203human GRCh38 chr11: 60,895,598-60,895,609 , GRCh37.p13 chr11: 60,663,070-60,663,081 PRPF19
    nsv4885672inversion1nstd200human GRCh37 chr11: 58,669,461-61,321,541 , GRCh38.p12 chr11: 58,901,988-61,554,069 , MS4A2, 118 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
    nsv4675148copy number variation1nstd102humanUncertain significance GRCh37 chr11: 60,385,382-62,456,278 , GRCh38.p12 chr11: 60,617,909-62,688,806 LOC105369326, MS4A18, 91 more genes
    nsv4457060copy number variation1nstd102humanUncertain significance GRCh37 chr11: 60,499,486-61,529,578 , GRCh38.p12 chr11: 60,732,013-61,762,106 TMEM109, LOC101927495, 41 more genes
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