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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148121copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,284,269-51,870,080 , GRCh38.p12 chr10: 45,788,821-50,110,320 LOC100420617, ZNF488, 108 more genes
    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
    nsv7093389copy number variation1nstd102humanUncertain significance GRCh37 chr10: 46,584,432-51,974,628 , GRCh38.p12 chr10: 45,931,517-50,214,868 NCOA4, AGAP7P, 106 more genes
    nsv7077381inversion1nstd229human GRCh38 chr10: 50,024,659-50,153,302 , GRCh37.p13 chr10|NW_004504302.1: 203,834-305,900 WASHC2A, FAM21EP, 2 more genes
    nsv7076978inversion1nstd229human GRCh38 chr10: 49,556,263-52,217,922 , GRCh37.p13 chr10: 50,764,309-53,977,682 A1CF, NPAP1P1, 36 more genes
    nsv7076661inversion1nstd229human GRCh38 chr10: 50,023,705-50,154,631 , GRCh37.p13 chr10|NW_004504302.1: 202,880-305,900 WASHC2A, FAM21EP, 2 more genes
    nsv7070353inversion1nstd229human GRCh38 chr10: 50,049,509-50,255,036 , GRCh37.p13 chr10: 51,886,486-52,014,796 ASAH2, WASHC2A, 2 more genes
    nsv7069878inversion1nstd229human GRCh38 chr10: 47,497,713-51,210,711 , GRCh37.p13 chr10: 46,591,857-52,970,471 MIR4294, SLC18A3, 76 more genes
    nsv7065178inversion1nstd229human GRCh38 chr10: 50,021,572-50,407,051 , GRCh37.p13 chr10: 51,886,486-52,166,811 SGMS1, WASHC2A, 5 more genes
    nsv7060309inversion1nstd229human GRCh38 chr10: 46,173,677-55,799,586 , GRCh37.p13 chr10: 46,591,857-57,559,346 NPY4R, LOC102724603, 138 more genes
    nsv7058135inversion1nstd229human GRCh38 chr10: 50,023,692-50,154,650 , GRCh37.p13 chr10|NW_004504302.1: 202,867-305,900 SLC9A3P3, SLC9A3P1, 2 more genes
    nsv6895769copy number variation1nstd229human GRCh38 chr10: 45,735,504-50,076,220 , GRCh37.p13 chr10: 46,591,857-51,028,871 , GRCh37.p13 chr10|NW_003871068.1: 6,619-2,281,126 BMS1P1, AGAP9, 108 more genes
    nsv6886834copy number variation1nstd229human GRCh38 chr10: 45,568,878-51,464,891 , GRCh37.p13 chr10: 46,064,326-53,224,651 PGBD3, MAPK8, 134 more genes
    nsv6885471copy number variation1nstd229human GRCh38 chr10: 48,691,383-50,476,716 , GRCh37.p13 chr10: 49,899,428-52,236,476 SLC18A3, LOC105378298, 35 more genes
    nsv6883183copy number variation1nstd229human GRCh38 chr10: 50,013,401-50,069,300 , GRCh37.p13 chr10|NW_004504302.1: 192,576-248,475 , GRCh37.p13 chr10: 51,773,161-51,829,060 WASHC2A, SLC9A3P3, 1 more genes
    nsv6880872copy number variation1nstd229human GRCh38 chr10: 50,022,626-50,407,050 , GRCh37.p13 chr10: 51,886,486-52,166,810 ASAH2, SLC9A3P1, 5 more genes
    nsv6637283copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 46,269,493-51,874,356 , GRCh38.p12 chr10: 45,774,045-50,114,596 CHAT, CTSLP2, 108 more genes
    nsv6635324copy number variation1nstd227human GRCh38.p12 chr10: 50,026,703-50,404,231 , GRCh37 chr10: 51,786,463-52,163,991 SLC9A3P1, ASAH2, 5 more genes
    nsv6620573copy number variation1nstd224human GRCh37 chr10: 51,782,026-51,912,644 , GRCh38.p12 chr10: 50,022,266-50,152,884 SLC9A3P1, WASHC2A, 2 more genes
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