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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141125copy number variation1nstd232human GRCh37.p13 chr11: 63,668,148-63,668,248 , GRCh38.p12 chr11: 63,900,676-63,900,776 MARK2
    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
    nsv7062901inversion1nstd229human GRCh38 chr11: 63,841,040-63,841,165 , GRCh37.p13 chr11: 63,608,512-63,608,637 MARK2
    nsv6916656copy number variation1nstd229human GRCh38 chr11: 63,842,339-63,875,244 , GRCh37.p13 chr11: 63,609,811-63,642,716 MARK2
    nsv6914037copy number variation1nstd229human GRCh38 chr11: 63,877,803-63,878,132 , GRCh37.p13 chr11: 63,645,275-63,645,604 MARK2
    nsv6908945copy number variation1nstd229human GRCh38 chr11: 63,881,805-63,982,372 , GRCh37.p13 chr11: 63,649,277-63,749,844 MARK2, NAA40, 5 more genes
    nsv6908311copy number variation1nstd229human GRCh38 chr11: 63,845,884-63,846,197 , GRCh37.p13 chr11: 63,613,356-63,613,669 MARK2
    nsv6906324copy number variation1nstd229human GRCh38 chr11: 63,901,401-63,938,000 , GRCh37.p13 chr11: 63,668,873-63,705,472 MARK2, RCOR2, 1 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
    nsv6904053copy number variation1nstd229human GRCh38 chr11: 63,879,723-63,881,884 , GRCh37.p13 chr11: 63,647,195-63,649,356 RNU6-1306P, MARK2
    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
    nsv6901214copy number variation1nstd229human GRCh38 chr11: 63,899,888-63,900,040 , GRCh37.p13 chr11: 63,667,360-63,667,512 MARK2
    nsv6593647inversion1nstd223human GRCh38 chr11: 63,859,679-63,860,388 , GRCh37.p13 chr11: 63,627,151-63,627,860 MARK2
    nsv6576058inversion1nstd223human GRCh38 chr11: 63,877,128-63,877,647 , GRCh37.p13 chr11: 63,644,600-63,645,119 MARK2
    nsv6472982copy number variation1nstd223human GRCh38 chr11: 63,858,141-63,861,810 , GRCh37.p13 chr11: 63,625,613-63,629,282 MARK2
    nsv6456940copy number variation1nstd223human GRCh38 chr11: 63,838,101-63,839,800 , GRCh37.p13 chr11: 63,605,573-63,607,272 MARK2
    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
    nsv6271368copy number variation1nstd214human GRCh38 chr11: 63,871,393-63,871,452 , GRCh37.p13 chr11: 63,638,865-63,638,924 MARK2
    nsv6189393copy number variation1nstd214human GRCh38 chr11: 63,871,305-63,871,364 , GRCh37.p13 chr11: 63,638,777-63,638,836 MARK2
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