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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7093700copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 120,905,748-120,905,865 , GRCh38.p12 chr10: 119,146,236-119,146,353 SFXN4
    nsv7076648inversion1nstd229human GRCh38 chr10: 119,076,083-120,210,505 , GRCh37.p13 chr10: 120,835,595-121,970,017 GRK5-IT1, RGS10, 23 more genes
    nsv7068192inversion1nstd229human GRCh38 chr10: 118,910,158-125,783,778 , GRCh37.p13 chr10: 120,669,670-127,472,347 CTBP2, RPS26P39, 114 more genes
    nsv6897954copy number variation1nstd229human GRCh38 chr10: 119,135,592-119,139,365 , GRCh37.p13 chr10: 120,895,104-120,898,877 SFXN4, DENND10
    nsv6896138copy number variation1nstd229human GRCh38 chr10: 118,899,347-119,334,149 , GRCh37.p13 chr10: 120,658,859-121,093,661 PRDX3, GRK5, 9 more genes
    nsv6889861copy number variation1nstd229human GRCh38 chr10: 119,164,030-119,168,960 , GRCh37.p13 chr10: 120,923,542-120,928,472 SFXN4, PRDX3
    nsv6888967copy number variation1nstd229human GRCh38 chr10: 119,138,969-119,216,525 , GRCh37.p13 chr10: 120,898,481-120,976,037 GRK5-IT1, PRDX3, 3 more genes
    nsv6880608copy number variation1nstd229human GRCh38 chr10: 119,143,745-119,145,573 , GRCh37.p13 chr10: 120,903,257-120,905,085 SFXN4
    nsv6879522copy number variation1nstd229human GRCh38 chr10: 119,148,801-119,171,400 , GRCh37.p13 chr10: 120,908,313-120,930,912 PRDX3, SFXN4
    nsv6590297inversion1nstd223human GRCh38 chr10: 119,163,640-119,164,048 , GRCh37.p13 chr10: 120,923,152-120,923,560 SFXN4
    nsv6586692inversion1nstd223human GRCh38 chr10: 119,151,296-119,151,756 , GRCh37.p13 chr10: 120,910,808-120,911,268 SFXN4
    nsv6585886inversion1nstd223human GRCh38 chr10: 118,910,158-125,783,778 , GRCh37.p13 chr10: 120,669,670-127,472,347 LOC105378520, SPADH, 114 more genes
    nsv6575621inversion1nstd223human GRCh38 chr10: 119,146,588-119,148,044 , GRCh37.p13 chr10: 120,906,100-120,907,556 SFXN4
    nsv6451810copy number variation1nstd223human GRCh38 chr10: 119,154,187-119,156,359 , GRCh37.p13 chr10: 120,913,699-120,915,871 SFXN4
    nsv6451467copy number variation1nstd223human GRCh38 chr10: 119,164,054-119,168,960 , GRCh37.p13 chr10: 120,923,566-120,928,472 PRDX3, SFXN4
    nsv6450643copy number variation1nstd223human GRCh38 chr10: 118,693,254-119,214,513 , GRCh37.p13 chr10: 120,452,766-120,974,025 SFXN4, DENND10, 11 more genes
    nsv6314129copy number variation1nstd102humanPathogenic GRCh37 chr10: 117,019,650-125,217,066 , GRCh38.p12 chr10: 115,260,173-123,457,550 PDZD8, MIR3663HG, 122 more genes
    nsv6314085copy number variation1nstd102humanPathogenic GRCh37 chr10: 108,455,687-135,427,143 , GRCh38.p12 chr10: 106,695,929-133,613,639 LOC107984268, DPYSL4, 379 more genes
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