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Items: 1 to 20 of 79

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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
    nsv6895651copy number variation1nstd229human GRCh38 chr10: 44,205,517-45,550,271 , GRCh37.p13 chr10: 44,700,965-46,045,719 OR13A1, RPL9P21, 27 more genes
    nsv6888354copy number variation1nstd229human GRCh38 chr10: 45,005,687-45,008,139 , GRCh37.p13 chr10: 45,501,135-45,503,587 ZNF22
    nsv6884219copy number variation1nstd229human GRCh38 chr10: 44,991,294-45,019,856 , GRCh37.p13 chr10: 45,486,742-45,515,304 RASSF4, ZNF22, 1 more genes
    nsv6883580copy number variation1nstd229human GRCh38 chr10: 42,792,424-46,796,570 , GRCh37.p13 chr10: 43,287,872-46,224,333 RASSF4, AGAP14P, 107 more genes
    nsv6442634copy number variation1nstd223human GRCh38 chr10: 44,991,294-45,019,856 , GRCh37.p13 chr10: 45,486,742-45,515,304 ZNF22-AS1, RASSF4, 1 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv5479407copy number variation1nstd206human GRCh38 chr10: 44,991,294-45,019,856 , GRCh37.p13 chr10: 45,486,742-45,515,304 ZNF22, RASSF4, 1 more genes
    nsv5035636inversion1nstd200human GRCh38 chr10: 32,580,256-50,959,654 , GRCh37.p13 chr10: 32,869,184-52,719,414 , ZNF32-AS2, 320 more genes
    nsv5033632inversion1nstd200human GRCh38 chr10: 36,819,152-58,318,428 , GRCh37.p13 chr10: 37,108,080-60,078,188 , LOC107001062, 306 more genes
    nsv4973594copy number variation1nstd200human GRCh38 chr10: 44,991,294-45,019,856 , GRCh37.p13 chr10: 45,486,742-45,515,304 ZNF22-AS1, RASSF4, 1 more genes
    nsv4973589copy number variation1nstd200human GRCh38 chr10: 44,650,256-45,337,855 , GRCh37.p13 chr10: 45,145,704-45,833,303 LOC105378281, OR13A1, 19 more genes
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4493179mobile element insertion1nstd166human GRCh37.p13 chr10: 45,495,291-45,495,291 , GRCh38.p12 chr10: 44,999,843-44,999,843 ZNF22, ZNF22-AS1
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4313384inversion1nstd166human GRCh37.p13 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , RET, 306 more genes
    nsv4172808copy number variation1nstd166human GRCh37.p13 chr10: 45,497,515-45,498,133 , GRCh38.p12 chr10: 45,002,067-45,002,685 ZNF22
    nsv3972353copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 37,149,872-46,169,876 , GRCh38.p12 chr10: 36,860,944-45,674,428 ALOX5, HNRNPF, 132 more genes
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