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Items: 1 to 20 of 277

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5972660insertion1nstd209human GRCh38 chr11: 94,426,429-94,426,429 , GRCh37.p13 chr11: 94,159,595-94,159,595 MRE11
    nsv5921405copy number variation1nstd209human GRCh38 chr11: 94,508,192-94,514,054 , GRCh37.p13 chr11: 94,241,358-94,247,220 C11orf97, MRE11
    nsv5918115copy number variation1nstd209human GRCh38 chr11: 94,426,414-94,426,465 , GRCh37.p13 chr11: 94,159,580-94,159,631 MRE11
    nsv5859689copy number variation1nstd209human GRCh38 chr11: 94,507,814-94,515,258 , GRCh37.p13 chr11: 94,240,980-94,248,424 MRE11, C11orf97
    nsv5713213mobile element insertion1nstd211human GRCh38 chr11: 94,466,792-94,466,792 , GRCh37.p13 chr11: 94,199,958-94,199,958 MIR548L, MRE11
    nsv5672787copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,180,375-94,180,614 , GRCh38.p12 chr11: 94,447,209-94,447,448 MRE11
    nsv5672786copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,168,988-94,170,411 , GRCh38.p12 chr11: 94,435,822-94,437,245 MRE11
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5653748insertion1nstd207human GRCh38 chr11: 94,426,429-94,426,429 , GRCh37.p13 chr11: 94,159,595-94,159,595 MRE11
    nsv5393956mobile element insertion1nstd206human GRCh38 chr11: 94,466,792-94,466,843 , GRCh37.p13 chr11: 94,199,958-94,200,009 MRE11, MIR548L
    nsv5380807copy number variation1nstd102humanUncertain significance GRCh37 chr11: 94,189,432-94,189,514 , GRCh38.p12 chr11: 94,456,266-94,456,348 MRE11
    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
    nsv5348135translocation1nstd200human GRCh38 chr11: 94,424,343-94,424,343 , GRCh38 chr11: 94,424,057-94,424,057 , GRCh37.p13 chr11: 94,157,223-94,157,223 , GRCh37.p13 chr11: 94,157,509-94,157,509 MRE11
    nsv5037979inversion1nstd200human GRCh38 chr11: 93,899,952-96,855,215 , GRCh37.p13 chr11: 93,633,118-96,726,215 , GPR83, 52 more genes
    nsv4971713copy number variation1nstd200human GRCh38 chr11: 94,468,118-94,468,202 , GRCh37.p13 chr11: 94,201,284-94,201,368 MRE11
    nsv4971712copy number variation1nstd200human GRCh38 chr11: 94,455,249-94,458,255 , GRCh37.p13 chr11: 94,188,415-94,191,421 MRE11
    nsv4971711copy number variation1nstd200human GRCh38 chr11: 94,452,440-94,453,956 , GRCh37.p13 chr11: 94,185,606-94,187,122 MRE11
    nsv4971710copy number variation1nstd200human GRCh38 chr11: 94,416,558-94,418,083 , GRCh37.p13 chr11: 94,149,724-94,151,249 MRE11
    nsv4971591copy number variation1nstd200human GRCh38 chr11: 91,285,470-94,799,390 , GRCh37.p13 chr11: 91,018,638-94,532,556 , LOC105369429, 53 more genes
    nsv4839969copy number variation1nstd200human GRCh37 chr11: 91,018,638-94,532,556 , GRCh38.p12 chr11: 91,285,470-94,799,390 , MIR548L, 53 more genes
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