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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077046inversion1nstd229human GRCh38 chr11: 15,063,537-15,175,187 , GRCh37.p13 chr11: 15,085,083-15,196,733 CALCB, INSC
    nsv7066313inversion1nstd229human GRCh38 chr11: 6,624,146-15,294,249 , GRCh37.p13 chr11: 6,645,377-15,315,795 RNA5SP332, TMEM41B, 163 more genes
    nsv7060162inversion1nstd229human GRCh38 chr11: 15,269,914-16,720,776 , GRCh37.p13 chr11: 15,291,460-16,742,323 INSC, SOX6, 10 more genes
    nsv7058428inversion1nstd229human GRCh38 chr11: 14,504,801-17,598,701 , GRCh37.p13 chr11: 14,526,347-17,620,248 RPL36AP37, LOC105376567, 41 more genes
    nsv6917151copy number variation1nstd229human GRCh38 chr11: 9,940,109-18,580,574 , GRCh37.p13 chr11: 9,961,656-18,602,121 MYOD1, MIR8070, 139 more genes
    nsv6916397copy number variation1nstd229human GRCh38 chr11: 15,156,656-15,157,397 , GRCh37.p13 chr11: 15,178,202-15,178,943 INSC
    nsv6915496copy number variation1nstd229human GRCh38 chr11: 15,127,404-15,136,699 , GRCh37.p13 chr11: 15,148,950-15,158,245 INSC
    nsv6915176copy number variation1nstd229human GRCh38 chr11: 15,241,164-15,241,246 , GRCh37.p13 chr11: 15,262,710-15,262,792 INSC
    nsv6915129copy number variation1nstd229human GRCh38 chr11: 15,223,563-15,242,662 , GRCh37.p13 chr11: 15,245,109-15,264,208 INSC
    nsv6915111copy number variation1nstd229human GRCh38 chr11: 15,242,104-15,242,726 , GRCh37.p13 chr11: 15,263,650-15,264,272 INSC
    nsv6914896copy number variation1nstd229human GRCh38 chr11: 14,922,661-15,132,639 , GRCh37.p13 chr11: 15,041,408-15,154,185 CALCA, CALCB, 2 more genes
    nsv6914505copy number variation1nstd229human GRCh38 chr11: 15,172,128-15,175,487 , GRCh37.p13 chr11: 15,193,674-15,197,033 INSC
    nsv6913766copy number variation1nstd229human GRCh38 chr11: 15,152,661-15,153,015 , GRCh37.p13 chr11: 15,174,207-15,174,561 INSC
    nsv6913336copy number variation1nstd229human GRCh38 chr11: 15,193,201-15,209,900 , GRCh37.p13 chr11: 15,214,747-15,231,446 INSC
    nsv6912828copy number variation1nstd229human GRCh38 chr11: 15,226,428-15,237,067 , GRCh37.p13 chr11: 15,247,974-15,258,613 INSC
    nsv6912223copy number variation1nstd229human GRCh38 chr11: 14,763,051-15,290,580 , GRCh37.p13 chr11: 14,784,597-15,312,126 CALCA, CYP2R1, 5 more genes
    nsv6911683copy number variation1nstd229human GRCh38 chr11: 15,255,977-15,256,165 , GRCh37.p13 chr11: 15,277,523-15,277,711 INSC
    nsv6911229copy number variation1nstd229human GRCh38 chr11: 15,144,683-15,145,121 , GRCh37.p13 chr11: 15,166,229-15,166,667 INSC
    nsv6910123copy number variation1nstd229human GRCh38 chr11: 15,248,201-15,256,900 , GRCh37.p13 chr11: 15,269,747-15,278,446 INSC
    nsv6908463copy number variation1nstd229human GRCh38 chr11: 15,194,610-15,199,445 , GRCh37.p13 chr11: 15,216,156-15,220,991 INSC
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