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Items: 1 to 20 of 69

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5598032copy number variation1nstd207human GRCh38 chr10: 42,869,603-42,869,654 , GRCh37.p13 chr10: 43,365,051-43,365,102 LINC02623
    nsv5593606copy number variation1nstd207human GRCh38 chr10: 42,869,595-42,869,714 , GRCh37.p13 chr10: 43,365,043-43,365,162 LINC02623
    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
    nsv4989029copy number variation1nstd200human GRCh38 chr10: 42,103,130-42,919,644 , GRCh37.p13 chr10: 42,598,578-43,415,092 LOC105378267, BMS1, 23 more genes
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4742953copy number variation1nstd199human GRCh37 chr10: 43,365,056-43,365,111 , GRCh38.p12 chr10: 42,869,608-42,869,663 LINC02623
    nsv4614777copy number variation1nstd183human GRCh37 chr10: 43,311,389-43,365,306 , GRCh38.p12 chr10: 42,815,941-42,869,858 LINC02623, RNU6-885P, 1 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
    nsv4183521copy number variation1nstd166human GRCh37.p13 chr10: 42,818,250-43,376,850 , GRCh38.p12 chr10: 42,322,802-42,881,402 ZNF37BP, CCNYL2, 18 more genes
    nsv4174554copy number variation1nstd166human GRCh37.p13 chr10: 43,365,118-43,365,192 , GRCh38.p12 chr10: 42,869,670-42,869,744 LINC02623
    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
    nsv3962567copy number variation1nstd168human GRCh38 chr10: 42,815,787-42,870,734 , GRCh37.p13 chr10: 43,311,235-43,366,182 BMS1, RNU6-885P, 1 more genes
    nsv3922833copy number variation1nstd102humanLikely benign NCBI36 chr10: 42,097,533-42,699,972 , GRCh37.p13 chr10: 42,777,527-43,379,966 , GRCh38.p12 chr10: 42,282,079-42,884,518 RSU1P1, DUXAP3, 18 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
    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
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