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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094183copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,146,421-75,283,128 , GRCh38.p12 chr11: 71,435,375-75,572,083 LOC112268078, LRTOMT, 142 more genes
    nsv7094108copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,148,848-71,148,999 , GRCh38.p12 chr11: 71,437,802-71,437,953 DHCR7
    nsv7094107copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,146,674-71,155,299 , GRCh38.p12 chr11: 71,435,628-71,444,253 DHCR7
    nsv7094014copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,152,249-71,153,318 , GRCh38.p12 chr11: 71,441,203-71,442,272 DHCR7
    nsv7076081inversion1nstd229human GRCh38 chr11: 71,432,629-71,433,924 , GRCh37.p13 chr11: 71,143,675-71,144,970 DHCR7
    nsv7075540inversion1nstd229human GRCh38 chr11: 67,968,443-71,626,784 , GRCh37.p13 chr11: 67,735,914-71,337,830 S100A11P3, CCND1, 76 more genes
    nsv7058265inversion1nstd229human GRCh38 chr11: 71,430,346-71,432,797 , GRCh37.p13 chr11: 71,141,392-71,143,843 DHCR7
    nsv6913831copy number variation1nstd229human GRCh38 chr11: 71,448,477-71,504,388 , GRCh37.p13 chr11: 71,159,523-71,215,434 MIR6754, NADSYN1, 2 more genes
    nsv6910186copy number variation1nstd229human GRCh38 chr11: 71,443,489-71,446,955 , GRCh37.p13 chr11: 71,154,535-71,158,001 DHCR7
    nsv6908275copy number variation1nstd229human GRCh38 chr11: 71,281,500-72,194,614 , GRCh37.p13 chr11: 71,088,949-71,905,658 DEFB130C, ANAPC15, 40 more genes
    nsv6904352copy number variation1nstd229human GRCh38 chr11: 71,435,842-71,437,810 , GRCh37.p13 chr11: 71,146,888-71,148,856 DHCR7
    nsv6637237copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,051,703-71,655,505 , GRCh38.p12 chr11: 71,340,657-71,944,459 FAM86C1P, KRTAP5-7, 28 more genes
    nsv6621132copy number variation1nstd224human GRCh37 chr11: 71,152,329-71,167,449 , GRCh38.p12 chr11: 71,441,283-71,456,403 NADSYN1, DHCR7
    nsv6462609copy number variation1nstd223human GRCh38 chr11: 71,443,489-71,446,952 , GRCh37.p13 chr11: 71,154,535-71,157,998 DHCR7
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6315267copy number variation1nstd102humanPathogenic GRCh38 chr11: 71,444,120-71,444,215 , GRCh37 chr11: 71,155,166-71,155,261 DHCR7
    nsv6309285copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,146,411-71,156,008 , GRCh38.p12 chr11: 71,435,365-71,444,962 DHCR7
    nsv6190157copy number variation1nstd214human GRCh38 chr11: 71,440,357-71,440,523 , GRCh37.p13 chr11: 71,151,403-71,151,569 DHCR7
    nsv6112744copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 71,155,018-71,156,024 , GRCh38.p12 chr11: 71,443,972-71,444,978 DHCR7
    nsv5915164copy number variation1nstd209human GRCh38 chr11: 71,439,704-71,447,532 , GRCh37.p13 chr11: 71,150,750-71,158,578 DHCR7
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