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Items: 1 to 20 of 275

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5892312copy number variation1nstd209human GRCh38 chr5: 10,458,576-10,458,663 , GRCh37.p13 chr5: 10,458,688-10,458,775 ROPN1L
    nsv5888246copy number variation1nstd209human GRCh38 chr5: 10,455,782-10,455,837 , GRCh37.p13 chr5: 10,455,894-10,455,949 ROPN1L
    nsv5638892insertion1nstd207human GRCh38 chr5: 10,458,682-10,458,682 , GRCh37.p13 chr5: 10,458,794-10,458,794 ROPN1L
    nsv5636875insertion1nstd207human GRCh38 chr5: 10,459,310-10,459,310 , GRCh37.p13 chr5: 10,459,422-10,459,422 ROPN1L
    nsv5635899insertion1nstd207human GRCh38 chr5: 10,474,880-10,474,880 , GRCh37.p13 chr5: 10,474,992-10,474,992 ROPN1L
    nsv5632257insertion1nstd207human GRCh38 chr5: 10,455,782-10,455,782 , GRCh37.p13 chr5: 10,455,894-10,455,894 ROPN1L
    nsv5630012insertion1nstd207human GRCh38 chr5: 10,471,046-10,471,046 , GRCh37.p13 chr5: 10,471,158-10,471,158 ROPN1L
    nsv5627402insertion1nstd207human GRCh38 chr5: 10,458,868-10,458,868 , GRCh37.p13 chr5: 10,458,980-10,458,980 ROPN1L
    nsv5550020insertion1nstd206human GRCh38 chr5: 10,459,385-10,459,395 , GRCh37.p13 chr5: 10,459,497-10,459,507 ROPN1L
    nsv5543633insertion1nstd206human GRCh38 chr5: 10,455,732-10,455,770 , GRCh37.p13 chr5: 10,455,844-10,455,882 ROPN1L
    nsv5463995copy number variation1nstd206human GRCh38 chr5: 10,479,592-10,479,647 , GRCh37.p13 chr5: 10,479,704-10,479,759 ROPN1L
    nsv5381771copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716 OTULINL, AKTIPP2, 317 more genes
    nsv4946475copy number variation1nstd200human GRCh38 chr5: 10,479,023-10,484,044 , GRCh37.p13 chr5: 10,479,135-10,484,156 ROPN1L
    nsv4946474copy number variation1nstd200human GRCh38 chr5: 10,442,504-10,445,590 , GRCh37.p13 chr5: 10,442,616-10,445,702 ROPN1L
    nsv4758240insertion1nstd199human GRCh37 chr5: 10,455,871-10,455,871 , GRCh38.p12 chr5: 10,455,759-10,455,759 ROPN1L
    nsv4753320insertion1nstd199human GRCh37 chr5: 10,458,985-10,458,985 , GRCh38.p12 chr5: 10,458,873-10,458,873 ROPN1L
    nsv4729667copy number variation1nstd102humanUncertain significance GRCh37 chr5: 10,382,918-10,611,579 , GRCh38.p12 chr5: 10,382,806-10,611,467 MIR10397, ROPN1L-AS1, 7 more genes
    nsv4728985copy number variation1nstd102humanUncertain significance GRCh37 chr5: 10,140,764-10,671,308 , GRCh38.p12 chr5: 10,140,652-10,671,196 MARCHF6, RPL30P7, 13 more genes
    nsv4685752copy number variation1nstd102humanPathogenic GRCh37 chr5: 71,904-22,078,969 , GRCh38.p12 chr5: 71,789-22,078,860 LINC01377, LOC100421308, 277 more genes
    nsv4674497copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-14,738,180 , GRCh38.p12 chr5: 113,461-14,738,071 LOC101929003, MTCYBP37, 192 more genes
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