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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv7075313inversion1nstd229human GRCh38 chr11: 62,887,478-63,793,002 , GRCh37.p13 chr11: 62,654,950-63,560,474 RPL29P22, TUBAP7, 25 more genes
    nsv7069560inversion1nstd229human GRCh38 chr11: 63,703,844-63,708,976 , GRCh37.p13 chr11: 63,471,316-63,476,448 RTN3
    nsv7064009inversion1nstd229human GRCh38 chr11: 63,716,404-63,739,173 , GRCh37.p13 chr11: 63,483,876-63,506,645 RTN3
    nsv7060800inversion1nstd229human GRCh38 chr11: 62,887,439-63,792,997 , GRCh37.p13 chr11: 62,654,911-63,560,469 TUBAP7, ATL3, 25 more genes
    nsv7058098inversion1nstd229human GRCh38 chr11: 62,887,432-63,795,073 , GRCh37.p13 chr11: 62,654,904-63,562,545 TUBAP7, ATL3, 25 more genes
    nsv6917878copy number variation1nstd229human GRCh38 chr11: 63,659,598-63,679,687 , GRCh37.p13 chr11: 63,427,070-63,447,159 ATL3, RTN3
    nsv6917640copy number variation1nstd229human GRCh38 chr11: 63,741,511-63,748,161 , GRCh37.p13 chr11: 63,508,983-63,515,633 RTN3
    nsv6914842copy number variation1nstd229human GRCh38 chr11: 63,684,902-63,688,500 , GRCh37.p13 chr11: 63,452,374-63,455,972 RTN3
    nsv6913604copy number variation1nstd229human GRCh38 chr11: 63,697,764-63,700,536 , GRCh37.p13 chr11: 63,465,236-63,468,008 RTN3
    nsv6912534copy number variation1nstd229human GRCh38 chr11: 63,696,224-63,700,918 , GRCh37.p13 chr11: 63,463,696-63,468,390 RTN3
    nsv6907970copy number variation1nstd229human GRCh38 chr11: 63,701,575-63,702,090 , GRCh37.p13 chr11: 63,469,047-63,469,562 RTN3
    nsv6907297copy number variation1nstd229human GRCh38 chr11: 63,690,201-63,697,100 , GRCh37.p13 chr11: 63,457,673-63,464,572 RTN3
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6905686copy number variation1nstd229human GRCh38 chr11: 63,724,731-63,727,573 , GRCh37.p13 chr11: 63,492,203-63,495,045 RTN3
    nsv6903780copy number variation1nstd229human GRCh38 chr11: 63,729,802-63,738,026 , GRCh37.p13 chr11: 63,497,274-63,505,498 RTN3
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    nsv6900440copy number variation1nstd229human GRCh38 chr11: 63,693,248-63,696,181 , GRCh37.p13 chr11: 63,460,720-63,463,653 RTN3
    nsv6898904copy number variation1nstd229human GRCh38 chr11: 63,707,561-63,711,035 , GRCh37.p13 chr11: 63,475,033-63,478,507 RTN3
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