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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137503insertion1nstd232human GRCh37.p13 chr11: 22,262,800-22,262,800 , GRCh38.p12 chr11: 22,241,254-22,241,254 ANO5
    nsv7093929copy number variation1nstd102humanUncertain significance GRCh37 chr11: 22,297,620-22,301,311 , GRCh38.p12 chr11: 22,276,074-22,279,765 ANO5
    nsv7093819copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 22,272,558-22,291,857 , GRCh38.p12 chr11: 22,251,012-22,270,311 ANO5
    nsv7093765copy number variation1nstd102humanPathogenic GRCh37 chr11: 22,261,095-22,261,250 , GRCh38.p12 chr11: 22,239,549-22,239,704 ANO5
    nsv7070460inversion1nstd229human GRCh38 chr11: 21,520,035-27,618,155 , GRCh37.p13 chr11: 21,541,581-27,639,702 RPS25P1, LOC105376598, 48 more genes
    nsv7069610inversion1nstd229human GRCh38 chr11: 22,191,800-22,191,982 , GRCh37.p13 chr11: 22,213,346-22,213,528 ANO5
    nsv7068237inversion1nstd229human GRCh38 chr11: 21,780,076-22,194,182 , GRCh37.p13 chr11: 21,801,622-22,215,728 ANO5, LOC102723370, 1 more genes
    nsv7058561inversion1nstd229human GRCh38 chr11: 22,022,654-22,865,606 , GRCh37.p13 chr11: 22,044,200-22,887,152 CCDC179, GAS2, 8 more genes
    nsv6917282copy number variation1nstd229human GRCh38 chr11: 22,199,301-22,232,400 , GRCh37.p13 chr11: 22,220,847-22,253,946 ANO5
    nsv6917022copy number variation1nstd229human GRCh38 chr11: 22,198,001-22,233,200 , GRCh37.p13 chr11: 22,219,547-22,254,746 ANO5
    nsv6916917copy number variation1nstd229human GRCh38 chr11: 22,270,201-22,313,100 , GRCh37.p13 chr11: 22,291,747-22,334,646 ANO5
    nsv6916912copy number variation1nstd229human GRCh38 chr11: 22,203,101-22,232,300 , GRCh37.p13 chr11: 22,224,647-22,253,846 ANO5
    nsv6916842copy number variation1nstd229human GRCh38 chr11: 22,202,501-22,232,900 , GRCh37.p13 chr11: 22,224,047-22,254,446 ANO5
    nsv6916655copy number variation1nstd229human GRCh38 chr11: 22,194,401-22,233,100 , GRCh37.p13 chr11: 22,215,947-22,254,646 ANO5
    nsv6916277copy number variation1nstd229human GRCh38 chr11: 22,153,601-22,258,600 , GRCh37.p13 chr11: 22,175,147-22,280,146 ANO5
    nsv6916150copy number variation1nstd229human GRCh38 chr11: 22,031,392-22,560,977 , GRCh37.p13 chr11: 22,052,938-22,582,523 SLC17A6, ANO5, 3 more genes
    nsv6915728copy number variation1nstd229human GRCh38 chr11: 22,197,001-22,234,800 , GRCh37.p13 chr11: 22,218,547-22,256,346 ANO5
    nsv6915185copy number variation1nstd229human GRCh38 chr11: 22,193,501-22,233,200 , GRCh37.p13 chr11: 22,215,047-22,254,746 ANO5
    nsv6915103copy number variation1nstd229human GRCh38 chr11: 22,153,901-22,256,200 , GRCh37.p13 chr11: 22,175,447-22,277,746 ANO5
    nsv6914460copy number variation1nstd229human GRCh38 chr11: 22,206,901-22,312,700 , GRCh37.p13 chr11: 22,228,447-22,334,246 ANO5
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