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Items: 1 to 20 of 116

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6917379copy number variation1nstd229human GRCh38 chr11: 65,074,458-65,080,289 , GRCh37.p13 chr11: 64,841,930-64,847,761 CDCA5
    nsv6915986copy number variation1nstd229human GRCh38 chr11: 64,935,377-65,143,014 , GRCh37.p13 chr11: 64,702,849-64,910,485 TM7SF2, HIGD1AP10, 19 more genes
    nsv6914187copy number variation1nstd229human GRCh38 chr11: 65,041,098-65,113,861 , GRCh37.p13 chr11: 64,808,570-64,881,333 TMEM262, TM7SF2, 5 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
    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
    nsv6900547copy number variation1nstd229human GRCh38 chr11: 65,065,542-65,073,233 , GRCh37.p13 chr11: 64,833,014-64,840,705 CDCA5
    nsv6470631copy number variation1nstd223human GRCh38 chr11: 64,935,377-65,143,014 , GRCh37.p13 chr11: 64,702,849-64,910,485 MAJIN, HIGD1AP10, 19 more genes
    nsv6459382copy number variation1nstd223human GRCh38 chr11: 65,070,610-65,071,117 , GRCh37.p13 chr11: 64,838,082-64,838,589 CDCA5
    nsv6458120copy number variation1nstd223human GRCh38 chr11: 65,040,220-65,093,556 , GRCh37.p13 chr11: 64,807,692-64,861,028 ZFPL1, NAALADL1, 5 more genes
    nsv6456023copy number variation1nstd223human GRCh38 chr11: 65,065,542-65,073,199 , GRCh37.p13 chr11: 64,833,014-64,840,671 CDCA5
    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
    nsv6309121copy number variation2nstd102humanPathogenic GRCh37 chr11: 64,522,783-66,283,694 , GRCh38.p12 chr11: 64,755,311-66,516,223 SF3B2, ZNRD2-DT, 124 more genes
    nsv6188101copy number variation1nstd214human GRCh38 chr11: 65,070,306-65,070,362 , GRCh37.p13 chr11: 64,837,778-64,837,834 CDCA5
    nsv6132269copy number variation1nstd213human GRCh37 chr11: 64,390,000-65,950,001 , GRCh38.p12 chr11: 64,622,528-66,182,530 MRPL49, CTSW, 103 more genes
    nsv6132112copy number variation1nstd213human GRCh37 chr11: 64,220,000-68,010,001 , GRCh38.p12 chr11: 64,452,528-68,242,533 ACTN3, ALDH3B1, 212 more genes
    nsv5512870copy number variation1nstd206human GRCh38 chr11: 65,070,310-65,070,363 , GRCh37.p13 chr11: 64,837,782-64,837,835 CDCA5
    nsv5503438copy number variation1nstd206human GRCh38 chr11: 65,080,887-65,081,052 , GRCh37.p13 chr11: 64,848,359-64,848,524 CDCA5
    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
    nsv5355288translocation1nstd200human GRCh38 chr11: 65,070,310-65,070,310 , GRCh38 chr11: 65,070,363-65,070,363 , GRCh37.p13 chr11: 64,837,782-64,837,782 , GRCh37.p13 chr11: 64,837,835-64,837,835 CDCA5
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