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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926685copy number variation1nstd209human GRCh38 chr11: 57,717,015-57,717,130 , GRCh37.p13 chr11: 57,484,487-57,484,602 TMX2, PPIAP42, 1 more genes
    nsv5922269copy number variation1nstd209human GRCh38 chr11: 57,734,874-57,736,625 , GRCh37.p13 chr11: 57,502,346-57,504,097 TMX2-CTNND1, TMX2
    nsv5914833copy number variation1nstd209human GRCh38 chr11: 57,776,396-57,777,043 , GRCh37.p13 chr11: 57,543,868-57,544,515 TMX2-CTNND1, CTNND1
    nsv5914325copy number variation1nstd209human GRCh38 chr11: 55,273,256-58,053,631 , GRCh37.p13 chr11: 55,040,732-57,821,103 , LOC107984365, 161 more genes
    nsv5848968copy number variation1nstd209human GRCh38 chr11: 57,734,864-57,736,663 , GRCh37.p13 chr11: 57,502,336-57,504,135 TMX2-CTNND1, TMX2
    nsv5672633copy number variation1nstd102humanPathogenic GRCh37 chr11: 57,471,510-57,564,464 , GRCh38.p12 chr11: 57,704,038-57,796,992 CTNND1, TMX2, 5 more genes
    nsv5672557copy number variation1nstd102humanPathogenic GRCh37 chr11: 57,558,951-57,583,780 , GRCh38.p12 chr11: 57,791,479-57,816,308 TMX2-CTNND1, CTNND1
    nsv5655897insertion1nstd207human GRCh38 chr11: 57,716,517-57,716,517 , GRCh37.p13 chr11: 57,483,989-57,483,989 TMX2, PPIAP42, 1 more genes
    nsv5602312copy number variation1nstd207human GRCh38 chr11: 57,717,015-57,717,130 , GRCh37.p13 chr11: 57,484,487-57,484,602 TMX2, PPIAP42, 1 more genes
    nsv5511343copy number variation1nstd206human GRCh38 chr11: 57,794,018-57,794,127 , GRCh37.p13 chr11: 57,561,490-57,561,599 CTNND1, TMX2-CTNND1
    nsv5507762copy number variation1nstd206human GRCh38 chr11: 57,734,861-57,736,673 , GRCh37.p13 chr11: 57,502,333-57,504,145 TMX2, TMX2-CTNND1
    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
    nsv5355206translocation1nstd200human GRCh38 chr11: 57,791,311-57,791,311 , GRCh38 chr11: 57,791,239-57,791,239 , GRCh37.p13 chr11: 57,558,783-57,558,783 , GRCh37.p13 chr11: 57,558,711-57,558,711 TMX2-CTNND1, CTNND1
    nsv5355205translocation1nstd200human GRCh38 chr11: 57,742,247-57,742,247 , GRCh38 chr11: 57,742,860-57,742,860 , GRCh37.p13 chr11: 57,510,332-57,510,332 , GRCh37.p13 chr11: 57,509,719-57,509,719 SELENOH, BTBD18, 1 more genes
    nsv5355204translocation1nstd200human GRCh38 chr11: 57,742,116-57,742,116 , GRCh38 chr11: 57,741,956-57,741,956 , GRCh37.p13 chr11: 57,509,428-57,509,428 , GRCh37.p13 chr11: 57,509,588-57,509,588 SELENOH, BTBD18, 1 more genes
    nsv5355203translocation1nstd200human GRCh38 chr11: 57,741,807-57,741,807 , GRCh38 chr11: 57,741,717-57,741,717 , GRCh37.p13 chr11: 57,509,279-57,509,279 , GRCh37.p13 chr11: 57,509,189-57,509,189 SELENOH, BTBD18, 1 more genes
    nsv5355202translocation1nstd200human GRCh38 chr11: 57,738,139-57,738,139 , GRCh38 chr11: 57,738,049-57,738,049 , GRCh37.p13 chr11: 57,505,521-57,505,521 , GRCh37.p13 chr11: 57,505,611-57,505,611 TMX2-CTNND1, TMX2
    nsv5355201translocation1nstd200human GRCh38 chr11: 57,734,913-57,734,913 , GRCh38 chr11: 57,736,617-57,736,617 , GRCh37.p13 chr11: 57,504,089-57,504,089 , GRCh37.p13 chr11: 57,502,385-57,502,385 TMX2, TMX2-CTNND1
    nsv5339693translocation1nstd200human GRCh37 chr11: 57,505,522-57,505,522 , GRCh37 chr11: 57,505,611-57,505,611 , GRCh38.p12 chr11: 57,738,139-57,738,139 , GRCh38.p12 chr11: 57,738,050-57,738,050 TMX2-CTNND1, TMX2
    nsv5330042translocation1nstd200human GRCh37 chr11: 57,493,371-57,493,371 , GRCh37 chr11: 57,493,189-57,493,189 , GRCh38.p12 chr11: 57,725,717-57,725,717 , GRCh38.p12 chr11: 57,725,899-57,725,899 TMX2, TMX2-CTNND1
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