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Items: 1 to 20 of 66

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5924103copy number variation1nstd209human GRCh38 chr10: 23,441,498-23,445,926 , GRCh37.p13 chr10: 23,730,427-23,734,855 OTUD1
    nsv5863296copy number variation1nstd209human GRCh38 chr10: 23,440,533-23,446,178 , GRCh37.p13 chr10: 23,729,462-23,735,107 OTUD1
    nsv5850623copy number variation1nstd209human GRCh38 chr10: 23,441,483-23,445,728 , GRCh37.p13 chr10: 23,730,412-23,734,657 OTUD1
    nsv5491709copy number variation1nstd206human GRCh38 chr10: 23,441,956-23,442,227 , GRCh37.p13 chr10: 23,730,885-23,731,156 OTUD1
    nsv5482966copy number variation1nstd206human GRCh38 chr10: 23,441,498-23,445,929 , GRCh37.p13 chr10: 23,730,427-23,734,858 OTUD1
    nsv5373241translocation1nstd200human GRCh38 chr10: 23,445,929-23,445,929 , GRCh38 chr10: 23,441,498-23,441,498 , GRCh37.p13 chr10: 23,734,858-23,734,858 , GRCh37.p13 chr10: 23,730,427-23,730,427 OTUD1
    nsv5316400copy number variation1nstd204human GRCh38.p13 chr10: 23,441,492-23,445,933 , GRCh37.p13 chr10: 23,730,421-23,734,862 OTUD1
    nsv5251068copy number variation1nstd204human GRCh38.p13 chr10: 23,442,779-23,445,528 , GRCh37.p13 chr10: 23,731,708-23,734,457 OTUD1
    nsv4983864copy number variation1nstd200human GRCh38 chr10: 23,441,956-23,442,226 , GRCh37.p13 chr10: 23,730,885-23,731,155 OTUD1
    nsv4843964copy number variation1nstd200human GRCh37 chr10: 23,730,427-23,734,858 , GRCh38.p12 chr10: 23,441,498-23,445,929 OTUD1
    nsv4829894copy number variation1nstd200human GRCh37 chr10: 23,730,885-23,731,156 , GRCh38.p12 chr10: 23,441,956-23,442,227 OTUD1
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4182677copy number variation1nstd166human GRCh37.p13 chr10: 23,730,885-23,731,155 , GRCh38.p12 chr10: 23,441,956-23,442,226 OTUD1
    nsv4175145copy number variation1nstd166human GRCh37.p13 chr10: 23,730,380-23,734,858 , GRCh38.p12 chr10: 23,441,451-23,445,929 OTUD1
    nsv3955764insertion1nstd168human GRCh38 chr10: 23,440,133-23,458,474 , GRCh37.p13 chr10: 23,729,062-23,747,403 OTUD1
    nsv3920796copy number variation1nstd102humanPathogenic NCBI36 chr10: 62,842-35,729,127 , GRCh37.p13 chr10: 72,842-35,689,121 , GRCh38.p12 chr10: 26,906-35,400,193 EPC1-AS1, RNU6-452P, 559 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
    nsv3917667copy number variation1nstd102humanPathogenic GRCh37 chr10: 224,406-26,628,907 , GRCh38 chr10: 90,205-26,339,978 , NCBI36 chr10: 126,145-26,668,913 RN7SKP241, DIP2C-AS1, 389 more genes
    nsv3911634copy number variation1nstd102humanLikely pathogenic NCBI36 chr10: 19,417,096-33,061,227 , GRCh37 chr10: 19,377,090-33,021,221 , GRCh38 chr10: 19,088,161-32,732,293 BMI1, CCND3P1, 221 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 LOC100419870, LOC102724439, 2105 more genes
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