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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112738copy number variation1nstd102humanPathogenic GRCh37 chr6: 149,619-3,951,208 , GRCh38.p12 chr6: 149,619-3,950,974 LINC01600, TUBB2BP1, 66 more genes
    nsv5966571insertion1nstd209human GRCh38 chr6: 1,054,032-1,054,032 , GRCh37.p13 chr6: 1,054,267-1,054,267 LINC01622
    nsv5965235insertion1nstd209human GRCh38 chr6: 974,079-974,079 , GRCh37.p13 chr6: 974,317-974,317 LINC01622
    nsv5905116copy number variation1nstd209human GRCh38 chr6: 1,003,914-1,003,972 , GRCh37.p13 chr6: 1,004,149-1,004,207 LINC01622
    nsv5903960copy number variation1nstd209human GRCh38 chr6: 982,398-1,004,786 , GRCh37.p13 chr6: 982,635-1,005,021 LINC01622
    nsv5899775copy number variation1nstd209human GRCh38 chr6: 994,166-994,278 , GRCh37.p13 chr6: 994,401-994,513 LINC01622
    nsv5894287copy number variation1nstd209human GRCh38 chr6: 1,018,714-1,019,074 , GRCh37.p13 chr6: 1,018,949-1,019,309 LINC01622
    nsv5846387copy number variation1nstd209human GRCh38 chr6: 982,499-1,004,947 , GRCh37.p13 chr6: 982,736-1,005,182 LINC01622
    nsv5845860copy number variation1nstd209human GRCh38 chr6: 984,901-986,134 , GRCh37.p13 chr6: 985,136-986,369 LINC01622
    nsv5681979mobile element insertion2nstd211human GRCh38 chr6: 1,018,054-1,018,054 , GRCh37.p13 chr6: 1,018,289-1,018,289 LINC01622
    nsv5678278mobile element insertion2nstd211human GRCh38 chr6: 1,009,236-1,009,236 , GRCh37.p13 chr6: 1,009,471-1,009,471 LINC01622
    nsv5675970mobile element insertion1nstd211human GRCh38 chr6: 975,789-975,789 , GRCh37.p13 chr6: 976,025-976,025 LINC01622
    nsv5642388insertion1nstd207human GRCh38 chr6: 994,274-994,274 , GRCh37.p13 chr6: 994,509-994,509 LINC01622
    nsv5633908insertion1nstd207human GRCh38 chr6: 993,981-993,981 , GRCh37.p13 chr6: 994,216-994,216 LINC01622
    nsv5629149insertion1nstd207human GRCh38 chr6: 1,053,787-1,053,787 , GRCh37.p13 chr6: 1,054,022-1,054,022 LINC01622
    nsv5626753insertion1nstd207human GRCh38 chr6: 1,051,553-1,051,553 , GRCh37.p13 chr6: 1,051,788-1,051,788 LINC01622
    nsv5625214insertion1nstd207human GRCh38 chr6: 1,009,227-1,009,227 , GRCh37.p13 chr6: 1,009,462-1,009,462 LINC01622
    nsv5582807copy number variation1nstd207human GRCh38 chr6: 1,003,914-1,003,972 , GRCh37.p13 chr6: 1,004,149-1,004,207 LINC01622
    nsv5553485insertion1nstd206human GRCh38 chr6: 1,007,114-1,007,116 , GRCh37.p13 chr6: 1,007,349-1,007,351 LINC01622
    nsv5473856copy number variation1nstd206human GRCh38 chr6: 1,018,714-1,019,075 , GRCh37.p13 chr6: 1,018,949-1,019,310 LINC01622
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