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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7075916inversion1nstd229human GRCh38 chr15: 75,241,707-77,965,147 , GRCh37.p13 chr15: 75,534,048-78,257,489 PTPN9, LOC105370902, 60 more genes
    nsv7075097inversion1nstd229human GRCh38 chr15: 77,775,775-77,775,821 , GRCh37.p13 chr15: 78,068,117-78,068,163 LINGO1
    nsv7070270inversion1nstd229human GRCh38 chr15: 70,870,846-78,233,029 , GRCh37.p13 chr15: 71,163,185-78,525,371 GOLGA6C, LOC102723657, 178 more genes
    nsv7064472inversion1nstd229human GRCh38 chr15: 73,034,378-79,475,825 , GRCh37.p13 chr15: 73,326,719-79,768,167 ANP32BP1, PSTPIP1, 169 more genes
    nsv7063463inversion1nstd229human GRCh38 chr15: 75,234,241-81,337,543 , GRCh37.p13 chr15: 75,526,582-81,629,884 RN7SL327P, LOC105370910, 138 more genes
    nsv7062257inversion1nstd229human GRCh38 chr15: 75,689,588-77,897,345 , GRCh37.p13 chr15: 75,981,929-78,189,687 KRT8P23, PSTPIP1, 37 more genes
    nsv7062055inversion1nstd229human GRCh38 chr15: 72,671,162-80,404,440 , GRCh37.p13 chr15: 72,963,503-80,696,782 MIR184, TRK-CTT16-1, 194 more genes
    nsv7060295inversion1nstd229human GRCh38 chr15: 75,736,549-77,907,855 , GRCh37.p13 chr15: 76,028,890-78,200,197 LOC105370906, RN7SL319P, 36 more genes
    nsv7058318inversion1nstd229human GRCh38 chr15: 75,735,884-77,868,867 , GRCh37.p13 chr15: 76,028,225-78,161,209 UBE2Q2, KRT8P23, 34 more genes
    nsv6977735copy number variation1nstd229human GRCh38 chr15: 77,795,490-77,801,528 , GRCh37.p13 chr15: 78,087,832-78,093,870 LINGO1
    nsv6977201copy number variation1nstd229human GRCh38 chr15: 77,717,301-77,720,300 , GRCh37.p13 chr15: 78,009,643-78,012,642 LINGO1
    nsv6975821copy number variation1nstd229human GRCh38 chr15: 77,784,380-77,787,595 , GRCh37.p13 chr15: 78,076,722-78,079,937 LINGO1
    nsv6974944copy number variation1nstd229human GRCh38 chr15: 77,786,313-77,793,727 , GRCh37.p13 chr15: 78,078,655-78,086,069 LINGO1
    nsv6972991copy number variation1nstd229human GRCh38 chr15: 77,774,654-78,040,840 , GRCh37.p13 chr15: 78,066,996-78,333,182 DNM1P9, LOC91450, 7 more genes
    nsv6972401copy number variation1nstd229human GRCh38 chr15: 77,739,872-78,051,654 , GRCh37.p13 chr15: 78,032,214-78,343,996 LINGO1, TBC1D2B, 7 more genes
    nsv6971852copy number variation1nstd229human GRCh38 chr15: 77,820,941-77,851,266 , GRCh37.p13 chr15: 78,113,283-78,143,608 LINGO1
    nsv6971399copy number variation1nstd229human GRCh38 chr15: 77,709,219-77,709,437 , GRCh37.p13 chr15: 78,001,561-78,001,779 LINGO1
    nsv6970713copy number variation1nstd229human GRCh38 chr15: 77,690,149-77,690,320 , GRCh37.p13 chr15: 77,982,491-77,982,662 LINGO1
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