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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971609insertion1nstd209human GRCh38 chr11: 18,579,004-18,579,004 , GRCh37.p13 chr11: 18,600,551-18,600,551 UEVLD
    nsv5915094copy number variation1nstd209human GRCh38 chr11: 18,424,161-18,537,002 , GRCh37.p13 chr11: 18,445,708-18,558,549 LDHAL6A, YWHABP2, 3 more genes
    nsv5912531copy number variation1nstd209human GRCh38 chr11: 18,580,587-18,580,880 , GRCh37.p13 chr11: 18,602,134-18,602,427 UEVLD
    nsv5909105copy number variation1nstd209human GRCh38 chr11: 18,584,644-18,600,213 , GRCh37.p13 chr11: 18,606,191-18,621,760 UEVLD, MTCH1P2, 2 more genes
    nsv5860860copy number variation1nstd209human GRCh38 chr11: 18,528,225-18,530,660 , GRCh37.p13 chr11: 18,549,772-18,552,207 UEVLD
    nsv5859945copy number variation1nstd209human GRCh38 chr11: 18,585,048-18,592,786 , GRCh37.p13 chr11: 18,606,595-18,614,333 UEVLD, LOC112268073, 1 more genes
    nsv5855492copy number variation1nstd209human GRCh38 chr11: 18,533,343-18,536,842 , GRCh37.p13 chr11: 18,554,890-18,558,389 UEVLD
    nsv5701718mobile element insertion2nstd211human GRCh38 chr11: 18,580,587-18,580,587 , GRCh37.p13 chr11: 18,602,134-18,602,134 UEVLD
    nsv5664371insertion1nstd207human GRCh38 chr11: 18,580,570-18,580,570 , GRCh37.p13 chr11: 18,602,117-18,602,117 UEVLD
    nsv5660812insertion1nstd207human GRCh38 chr11: 18,560,100-18,560,100 , GRCh37.p13 chr11: 18,581,647-18,581,647 UEVLD
    nsv5553881insertion1nstd206human GRCh38 chr11: 18,528,346-18,528,346 , GRCh37.p13 chr11: 18,549,893-18,549,893 UEVLD
    nsv5540458insertion1nstd206human GRCh38 chr11: 18,560,130-18,560,149 , GRCh37.p13 chr11: 18,581,677-18,581,696 UEVLD
    nsv5510357copy number variation1nstd206human GRCh38 chr11: 18,527,181-18,527,970 , GRCh37.p13 chr11: 18,548,728-18,549,517 TSG101, UEVLD
    nsv5507673copy number variation1nstd206human GRCh38 chr11: 16,359,999-20,627,000 , GRCh37.p13 chr11: 16,381,545-20,648,546 , CSRP3, 102 more genes
    nsv5507183copy number variation1nstd206human GRCh38 chr11: 18,572,000-18,578,000 , GRCh37.p13 chr11: 18,593,547-18,599,547 UEVLD
    nsv5506669copy number variation1nstd206human GRCh38 chr11: 18,578,953-18,582,961 , GRCh37.p13 chr11: 18,600,500-18,604,508 UEVLD
    nsv5501133copy number variation1nstd206human GRCh38 chr11: 18,584,624-18,600,267 , GRCh37.p13 chr11: 18,606,171-18,621,814 UEVLD, MISFA, 2 more genes
    nsv5494629copy number variation1nstd206human GRCh38 chr11: 18,549,954-18,556,417 , GRCh37.p13 chr11: 18,571,501-18,577,964 UEVLD
    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
    nsv5380720copy number variation1nstd102humanUncertain significance GRCh37 chr11: 17,552,691-19,213,995 , GRCh38.p12 chr11: 17,531,144-19,192,448 USH1C, HIGD1AP5, 53 more genes
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