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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5355297translocation1nstd200human GRCh38 chr11: 65,890,571-65,890,571 , GRCh38 chr11: 65,890,507-65,890,507 , GRCh37.p13 chr11: 65,658,042-65,658,042 , GRCh37.p13 chr11: 65,657,978-65,657,978 FOSL1, CCDC85B
    nsv5344397translocation1nstd200human GRCh37 chr11: 65,658,042-65,658,042 , GRCh37 chr11: 65,657,978-65,657,978 , GRCh38.p12 chr11: 65,890,571-65,890,571 , GRCh38.p12 chr11: 65,890,507-65,890,507 CCDC85B, FOSL1
    nsv5277798copy number variation1nstd204human GRCh38.p13 chr11: 65,676,501-66,823,500 , GRCh37.p13 chr11: 65,443,972-66,590,971 , BBS1, 68 more genes
    nsv5264980copy number variation1nstd204human GRCh38.p13 chr11: 65,876,001-66,092,800 , GRCh37.p13 chr11: 65,643,472-65,860,271 , LOC100420020, 17 more genes
    nsv5262794copy number variation1nstd204human GRCh37.p13 chr11: 65,642,172-65,707,071 , GRCh38.p13 chr11: 65,874,701-65,939,600 , CTSW, 6 more genes
    nsv4979859copy number variation1nstd200human GRCh38 chr11: 65,893,443-65,893,570 , GRCh37.p13 chr11: 65,660,914-65,661,041 FOSL1
    nsv4844423copy number variation1nstd200human GRCh37 chr11: 65,660,914-65,661,041 , GRCh38.p12 chr11: 65,893,443-65,893,570 FOSL1
    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
    nsv4453555copy number variation1nstd102humanUncertain significance GRCh38 chr11: 65,866,431-66,347,555 , GRCh37 chr11: 65,633,902-66,115,026 CNIH2, YIF1A, 33 more genes
    nsv4349000copy number variation1nstd102humanPathogenic GRCh37 chr11: 65,138,976-67,574,402 , GRCh38.p12 chr11: 65,371,505-67,806,931 SNORD13F, ZNRD2, 141 more genes
    nsv4199742copy number variation1nstd166human GRCh37.p13 chr11: 65,654,000-65,659,500 , GRCh38.p12 chr11: 65,886,529-65,892,029 FOSL1, CCDC85B, 1 more genes
    nsv4199257copy number variation1nstd166human GRCh37.p13 chr11: 65,657,978-65,658,042 , GRCh38.p12 chr11: 65,890,507-65,890,571 FOSL1, CCDC85B
    nsv4193897copy number variation1nstd166human GRCh37.p13 chr11: 65,662,380-65,662,883 , GRCh38.p12 chr11: 65,894,909-65,895,412 FOSL1
    nsv3961647insertion1nstd168human GRCh38 chr11: 65,872,258-65,989,242 , GRCh37.p13 chr11: 65,639,729-65,756,713 , SART1, 10 more genes
    nsv3957413copy number variation1nstd168human GRCh38 chr11: 65,860,810-65,919,961 , GRCh37.p13 chr11: 65,628,281-65,687,432 CTSW, FOSL1, 6 more genes
    nsv3921639copy number variation1nstd102humanPathogenic NCBI36 chr11: 65,265,478-67,229,716 , GRCh37 chr11: 65,508,902-67,473,140 , GRCh38 chr11: 65,741,431-67,705,669 MIR6860, DOC2GP, 106 more genes
    nsv3919463copy number variation1nstd102humanUncertain significance GRCh37 chr11: 65,649,068-65,661,361 , NCBI36 chr11: 65,405,644-65,417,937 , GRCh38 chr11: 65,881,597-65,893,890 CTSW, FOSL1, 2 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
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