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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5924678copy number variation1nstd209human GRCh38 chr11: 110,156,113-110,156,165 , GRCh37.p13 chr11: 110,026,838-110,026,890 ZC3H12C
    nsv5911027copy number variation1nstd209human GRCh38 chr11: 110,105,974-110,106,299 , GRCh37.p13 chr11: 109,976,699-109,977,024 ZC3H12C
    nsv5725255mobile element insertion1nstd211human GRCh38 chr11: 110,118,403-110,118,403 , GRCh37.p13 chr11: 109,989,128-109,989,128 ZC3H12C
    nsv5713662mobile element insertion2nstd211human GRCh38 chr11: 110,154,852-110,154,852 , GRCh37.p13 chr11: 110,025,577-110,025,577 ZC3H12C
    nsv5708100mobile element insertion1nstd211human GRCh38 chr11: 110,162,181-110,162,181 , GRCh37.p13 chr11: 110,032,906-110,032,906 ZC3H12C
    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
    nsv5602527copy number variation1nstd207human GRCh38 chr11: 110,156,113-110,156,165 , GRCh37.p13 chr11: 110,026,838-110,026,890 ZC3H12C
    nsv5588767copy number variation1nstd207human GRCh38 chr11: 110,105,974-110,106,299 , GRCh37.p13 chr11: 109,976,699-109,977,024 ZC3H12C
    nsv5559227mobile element insertion1nstd206human GRCh38 chr11: 110,118,403-110,118,454 , GRCh37.p13 chr11: 109,989,128-109,989,179 ZC3H12C
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 more genes
    nsv5505568copy number variation1nstd206human GRCh38 chr11: 110,105,987-110,106,300 , GRCh37.p13 chr11: 109,976,712-109,977,025 ZC3H12C
    nsv5504455copy number variation1nstd206human GRCh38 chr11: 110,156,113-110,156,169 , GRCh37.p13 chr11: 110,026,838-110,026,894 ZC3H12C
    nsv5407157mobile element insertion1nstd206human GRCh38 chr11: 110,162,181-110,162,225 , GRCh37.p13 chr11: 110,032,906-110,032,950 ZC3H12C
    nsv5382999mobile element deletion2nstd186human GRCh37 chr11: 109,976,712-109,977,025 , GRCh38.p12 chr11: 110,105,987-110,106,300 ZC3H12C
    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
    nsv5348278translocation1nstd200human GRCh38 chr11: 110,156,113-110,156,113 , GRCh38 chr11: 110,156,169-110,156,169 , GRCh37.p13 chr11: 110,026,838-110,026,838 , GRCh37.p13 chr11: 110,026,894-110,026,894 ZC3H12C
    nsv5330086translocation1nstd200human GRCh37 chr11: 110,026,838-110,026,838 , GRCh37 chr11: 110,026,894-110,026,894 , GRCh38.p12 chr11: 110,156,169-110,156,169 , GRCh38.p12 chr11: 110,156,113-110,156,113 ZC3H12C
    nsv5325521translocation1nstd204human GRCh38.p13 chr11: 110,156,113-110,156,113 , GRCh38.p13 chr11: 110,156,169-110,156,169 , GRCh37.p13 chr11: 110,026,838-110,026,838 , GRCh37.p13 chr11: 110,026,894-110,026,894 ZC3H12C
    nsv5266783copy number variation1nstd204human GRCh38.p13 chr11: 110,106,001-110,106,300 , GRCh37.p13 chr11: 109,976,726-109,977,025 ZC3H12C
    nsv5212906mobile element deletion1nstd204human GRCh38.p13 chr11: 110,105,987-110,106,300 , GRCh37.p13 chr11: 109,976,712-109,977,025 ZC3H12C
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