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Items: 1 to 20 of 68

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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
    nsv6894474copy number variation1nstd229human GRCh38 chr10: 23,342,631-23,343,799 , GRCh37.p13 chr10: 23,631,560-23,632,728 C10orf67-AS1, C10orf67
    nsv6893684copy number variation1nstd229human GRCh38 chr10: 23,343,721-23,368,031 , GRCh37.p13 chr10: 23,632,650-23,656,960 C10orf67-AS1, C10orf67
    nsv6885272copy number variation1nstd229human GRCh38 chr10: 23,332,980-23,343,252 , GRCh37.p13 chr10: 23,621,909-23,632,181 C10orf67-AS1, C10orf67
    nsv6881619copy number variation1nstd229human GRCh38 chr10: 23,324,592-23,350,487 , GRCh37.p13 chr10: 23,613,521-23,639,416 C10orf67, C10orf67-AS1
    nsv6452011copy number variation1nstd223human GRCh38 chr10: 23,340,342-23,374,883 , GRCh37.p13 chr10: 23,629,271-23,663,812 C10orf67, C10orf67-AS1
    nsv6447208copy number variation1nstd223human GRCh38 chr10: 23,343,846-23,344,122 , GRCh37.p13 chr10: 23,632,775-23,633,051 C10orf67-AS1, C10orf67
    nsv6438918copy number variation1nstd223human GRCh38 chr10: 23,324,592-23,350,487 , GRCh37.p13 chr10: 23,613,521-23,639,416 C10orf67, C10orf67-AS1
    nsv6313952copy number variation1nstd102humanPathogenic GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593 RPL36AP55, HNRNPA1P32, 418 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
    nsv6132031copy number variation1nstd213human GRCh37 chr10: 18,100,000-28,260,001 , GRCh38.p12 chr10: 17,839,748-27,971,072 BMI1, CACNB2, 136 more genes
    nsv6131951copy number variation1nstd213human GRCh37 chr10: 23,520,000-23,860,001 , GRCh38.p12 chr10: 23,231,071-23,571,072 OTUD1, C10orf67, 2 more genes
    nsv6086764insertion1nstd212human GRCh38 chr10: 23,342,007-23,342,007 , GRCh37.p13 chr10: 23,630,936-23,630,936 C10orf67-AS1, C10orf67
    nsv4975399copy number variation1nstd200human GRCh38 chr10: 23,345,060-23,345,191 , GRCh37.p13 chr10: 23,633,989-23,634,120 C10orf67, C10orf67-AS1
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    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
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