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Items: 1 to 20 of 229

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976211insertion1nstd209human GRCh38 chr11: 108,131,354-108,131,354 , GRCh37.p13 chr11: 108,002,081-108,002,081 ACAT1
    nsv5918104copy number variation1nstd209human GRCh38 chr11: 104,190,618-110,044,159 , GRCh37.p13 chr11: 104,061,346-109,914,884 , CARD18, 71 more genes
    nsv5911774copy number variation1nstd209human GRCh38 chr11: 108,099,164-108,119,362 , GRCh37.p13 chr11: 107,969,891-107,990,089 ACAT1, CUL5
    nsv5848990copy number variation1nstd209human GRCh38 chr11: 108,106,122-108,119,109 , GRCh37.p13 chr11: 107,976,849-107,989,836 CUL5, ACAT1
    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
    nsv5672615copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 108,004,537-108,005,053 , GRCh38.p12 chr11: 108,133,810-108,134,326 ACAT1
    nsv5672614copy number variation1nstd102humanPathogenic GRCh37 chr11: 107,992,324-107,992,415 , GRCh38.p12 chr11: 108,121,597-108,121,688 ACAT1
    nsv5672539copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 108,009,615-108,009,778 , GRCh38.p12 chr11: 108,138,888-108,139,051 ACAT1
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 more genes
    nsv5508112copy number variation1nstd206human GRCh38 chr11: 108,136,125-108,136,195 , GRCh37.p13 chr11: 108,006,852-108,006,922 ACAT1
    nsv5505486copy number variation1nstd206human GRCh38 chr11: 108,133,010-108,134,867 , GRCh37.p13 chr11: 108,003,737-108,005,594 ACAT1
    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
    nsv5373861translocation1nstd200human GRCh38 chr11: 108,127,718-108,127,718 , GRCh38 chr11: 108,129,171-108,129,171 , GRCh37.p13 chr11: 107,999,898-107,999,898 , GRCh37.p13 chr11: 107,998,445-107,998,445 ACAT1
    nsv5373860translocation1nstd200human GRCh38 chr11: 108,127,710-108,127,710 , GRCh38 chr11: 108,128,979-108,128,979 , GRCh37.p13 chr11: 107,998,437-107,998,437 , GRCh37.p13 chr11: 107,999,706-107,999,706 ACAT1
    nsv5373859translocation1nstd200human GRCh38 chr11: 108,044,676-108,044,676 , GRCh38 chr11: 108,131,824-108,131,824 , GRCh37.p13 chr11: 108,002,551-108,002,551 , GRCh37.p13 chr11: 107,915,403-107,915,403 ACAT1, CUL5
    nsv5334623translocation1nstd200human GRCh37 chr11: 108,002,551-108,002,551 , GRCh37 chr11: 107,915,403-107,915,403 , GRCh38.p12 chr11: 108,131,824-108,131,824 , GRCh38.p12 chr11: 108,044,676-108,044,676 CUL5, ACAT1
    nsv5324746translocation1nstd204human GRCh37.p13 chr11: 108,002,551-108,002,551 , GRCh37.p13 chr11: 107,915,403-107,915,403 , GRCh38.p13 chr11: 108,044,676-108,044,676 , GRCh38.p13 chr11: 108,131,824-108,131,824 ACAT1, CUL5
    nsv5261007copy number variation1nstd204human GRCh38.p13 chr11: 108,044,601-108,133,700 , GRCh37.p13 chr11: 107,915,328-108,004,427 ACAT1, CUL5
    nsv5060043delins1nstd102humanPathogenic GRCh37 chr11: 108,003,055-108,012,264 , GRCh38 chr11: 108,132,328-108,141,537 ACAT1
    nsv4989284copy number variation1nstd200human GRCh38 chr11: 108,112,343-108,134,992 , GRCh37.p13 chr11: 107,983,070-108,005,719 ACAT1
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