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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
    nsv7098865copy number variation1nstd102humanLikely pathogenic GRCh37.p13 chr10|NW_003871068.1: 1-2,281,126 , GRCh38 chr10: 45,704,708-50,015,268 , GRCh37.p13 chr10: 46,200,156-51,028,871 CHAT, CTSLP2, 107 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
    nsv7069878inversion1nstd229human GRCh38 chr10: 47,497,713-51,210,711 , GRCh37.p13 chr10: 46,591,857-52,970,471 MIR4294, SLC18A3, 76 more genes
    nsv7066519inversion1nstd229human GRCh38 chr10: 45,802,941-50,026,843 , GRCh37.p13 chr10|NW_003871068.1: 74,056-2,281,126 , GRCh37.p13 chr10: 46,591,857-51,028,871 RNA5SP317, AHCYP1, 106 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
    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
    nsv6637718copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 46,966,534-51,700,837 , GRCh38.p12 chr10: 45,931,517-49,929,364 CHAT, CTSLP2, 96 more genes
    nsv6637431copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 48,252,675-51,861,565 , GRCh38.p12 chr10: 45,999,930-49,959,916 CHAT, CTSLP2, 95 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
    nsv6637162copy number variation1nstd102humanUncertain significance GRCh37 chr10: 47,062,985-48,769,625 , GRCh38.p12 chr10: 46,157,935-47,923,579 AHCYP1, SHLD2P3, 51 more genes
    nsv6635526copy number variation2nstd227human GRCh38.p12 chr10: 45,788,238-47,923,579 , GRCh37 chr10: 46,283,686-47,703,869 CTSLP2, GDF2, 65 more genes
    nsv6634443copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,287,821-51,627,470 , GRCh38.p12 chr10: 45,792,373-49,929,364 GLUD1P2, RBP3, 100 more genes
    nsv6620634copy number variation1nstd224human GRCh37 chr10: 47,543,322-48,340,623 , GRCh38.p12 chr10: 47,398,739-47,986,452 CTSLP2, SHLD2P3, 17 more genes
    nsv6620626copy number variation3nstd224human GRCh37 chr10: 47,087,499-47,703,869 , GRCh38.p12 chr10: 46,157,935-47,923,579 GDF10, RBP3, 51 more genes
    nsv6620613copy number variation1nstd224human GRCh37 chr10: 46,965,755-47,703,946 , GRCh38.p12 chr10: 46,157,935-47,923,579 RHEBP1, SYT15, 51 more genes
    nsv6620567copy number variation2nstd224human GRCh37 chr10: 47,074,201-47,703,869 , GRCh38.p12 chr10: 46,157,935-47,923,579 GDF10, RBP3, 51 more genes
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