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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926471copy number variation1nstd209human GRCh38 chr11: 64,863,933-64,865,372 , GRCh37.p13 chr11: 64,631,405-64,632,844 EHD1
    nsv5916439copy number variation1nstd209human GRCh38 chr11: 64,855,856-64,855,951 , GRCh37.p13 chr11: 64,623,328-64,623,423 EHD1
    nsv5911506copy number variation1nstd209human GRCh38 chr11: 64,867,547-64,886,490 , GRCh37.p13 chr11: 64,635,019-64,653,962 EHD1, MIR10392, 2 more genes
    nsv5853640copy number variation1nstd209human GRCh38 chr11: 64,867,433-64,884,895 , GRCh37.p13 chr11: 64,634,905-64,652,367 RPS16P6, EHD1, 1 more genes
    nsv5593879copy number variation1nstd207human GRCh38 chr11: 64,855,856-64,855,951 , GRCh37.p13 chr11: 64,623,328-64,623,423 EHD1
    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
    nsv5333446translocation1nstd200human GRCh37 chr11: 64,635,471-64,635,471 , GRCh37 chr11: 64,635,972-64,635,972 , GRCh38.p12 chr11: 64,867,999-64,867,999 , GRCh38.p12 chr11: 64,868,500-64,868,500 EHD1
    nsv5267852copy number variation1nstd204human GRCh38.p13 chr11: 64,173,401-65,676,300 , GRCh37.p13 chr11: 63,940,873-65,443,771 , TALAM1, 103 more genes
    nsv4985046copy number variation1nstd200human GRCh38 chr11: 64,868,004-64,868,745 , GRCh37.p13 chr11: 64,635,476-64,636,217 EHD1
    nsv4985045copy number variation1nstd200human GRCh38 chr11: 64,845,523-64,919,251 , GRCh37.p13 chr11: 64,612,995-64,686,723 MIR6750, ATG2A, 8 more genes
    nsv4848356copy number variation1nstd200human GRCh37 chr11: 64,635,476-64,636,217 , GRCh38.p12 chr11: 64,868,004-64,868,745 EHD1
    nsv4843148copy number variation1nstd200human GRCh37 chr11: 64,633,210-64,633,302 , GRCh38.p12 chr11: 64,865,738-64,865,830 EHD1
    nsv4834834copy number variation1nstd200human GRCh37 chr11: 64,631,341-64,632,885 , GRCh38.p12 chr11: 64,863,869-64,865,413 EHD1
    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
    nsv4737609copy number variation1nstd199human GRCh37 chr11: 64,623,337-64,623,433 , GRCh38.p12 chr11: 64,855,865-64,855,961 EHD1
    nsv4679239copy number variation1nstd189human GRCh37.p13 chr11: 64,222,931-65,140,850 , GRCh38.p12 chr11: 64,455,459-65,373,379 ARL2, VPS51, 52 more genes
    nsv4604563copy number variation1nstd183human GRCh37 chr11: 64,645,373-64,646,642 , GRCh38.p12 chr11: 64,877,901-64,879,170 EHD1, MIR10392
    nsv4575077mobile element insertion1nstd166human GRCh37.p13 chr11: 64,620,209-64,620,209 , GRCh38.p12 chr11: 64,852,737-64,852,737 EHD1
    nsv4456749copy number variation1nstd102humanUncertain significance GRCh37 chr11: 64,396,501-64,883,447 , GRCh38.p12 chr11: 64,629,029-65,115,975 EHD1, TM7SF2, 32 more genes
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