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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv3923539inversion1nstd102humanLikely pathogenic GRCh38.p12 chr10: 43,115,743-59,903,521 , GRCh37 chr10: 43,611,191-61,663,279 ALOX5, CHAT, 248 more genes
    nsv3921181copy number variation1nstd102humanPathogenic NCBI36 chr10: 41,927,641-68,830,439 , GRCh38 chr10: 42,112,187-67,400,675 , GRCh37 chr10: 42,607,635-69,160,433 AGAP6, A1CF, 338 more genes
    nsv3920598copy number variation1nstd102humanBenign NCBI36 chr10: 4,636,926-47,125,152 , GRCh38 chr10: 4,604,734-48,074,662 , GRCh37 chr10: 4,646,926-47,531,169 LOC100420467, LOC105376474, 709 more genes
    nsv3920534copy number variation1nstd102humanUncertain significance NCBI36 chr10: 44,725,032-44,938,989 , GRCh37.p13 chr10: 45,405,026-45,618,983 , GRCh38.p12 chr10: 44,909,578-45,123,535 CEP164P1, LOC105378281, 9 more genes
    nsv3919301copy number variation1nstd102humanPathogenic NCBI36 chr10: 43,277,502-55,351,191 , GRCh37.p13 chr10: 43,957,496-55,681,185 , GRCh38.p12 chr10: 38,980,309-49,959,916 FAM245B, NPY4R2, 196 more genes
    nsv3918611copy number variation1nstd102humanPathogenic GRCh38 chr10: 42,395,201-50,877,059 , NCBI36 chr10: 42,210,655-52,306,825 , GRCh37 chr10: 42,890,649-52,636,819 LOC105378289, FAM170B-AS1, 211 more genes
    nsv3917047copy number variation1nstd102humanPathogenic NCBI36 chr10: 42,500,760-75,145,672 , GRCh37 chr10: 43,180,754-75,475,666 , GRCh38 chr10: 42,685,306-73,715,908 SLC9A3P3, JMJD1C-AS2, 476 more genes
    nsv3916253copy number variation1nstd102humanPathogenic GRCh38 chr10: 42,884,294-52,265,317 , NCBI36 chr10: 42,699,748-53,695,083 , GRCh37 chr10: 43,379,742-54,025,077 PTPN20CP, ASAH2, 198 more genes
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