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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
    nsv5561752sequence alteration1nstd206human GRCh38 chr14: 23,629,192-23,629,195 , GRCh37.p13 chr14: 24,098,401-24,098,404 DHRS2
    nsv5497432copy number variation1nstd206human GRCh38 chr14: 23,632,719-23,633,919 , GRCh37.p13 chr14: 24,101,928-24,103,128 DHRS2
    nsv5318939copy number variation1nstd204human GRCh38.p13 chr14: 23,632,747-23,633,884 , GRCh37.p13 chr14: 24,101,956-24,103,093 DHRS2
    nsv5185220mobile element insertion1nstd203human GRCh38 chr14: 23,635,507-23,635,523 , GRCh37.p13 chr14: 24,104,716-24,104,732 DHRS2
    nsv4990868copy number variation1nstd200human GRCh38 chr14: 23,632,755-23,633,879 , GRCh37.p13 chr14: 24,101,964-24,103,088 DHRS2
    nsv4842147copy number variation1nstd200human GRCh37 chr14: 24,101,964-24,103,088 , GRCh38.p12 chr14: 23,632,755-23,633,879 DHRS2
    nsv4685750copy number variation1nstd102humannot provided GRCh37 chr14: 20,511,672-42,881,888 , GRCh38.p12 chr14: 20,043,513-42,412,685 IGBP1P1, RAB2B, 579 more genes
    nsv4675943copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-44,829,030 , GRCh38.p12 chr14: 20,043,513-44,359,827 TRAJ36, SEC23A-AS1, 590 more genes
    nsv4675720copy number variation1nstd102humanUncertain significance GRCh37 chr14: 24,080,270-24,151,630 , GRCh38.p12 chr14: 23,611,061-23,682,421 DHRS2, LOC105370407
    nsv4349901copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,100,682-28,730,087 , GRCh38.p12 chr14: 18,324,205-28,260,881 TRAV4, UNGP2, 458 more genes
    nsv4224521copy number variation1nstd166human GRCh37.p13 chr14: 24,101,964-24,103,088 , GRCh38.p12 chr14: 23,632,755-23,633,879 DHRS2
    nsv3934686insertion1nstd167human GRCh37 chr14: 24,098,399-24,098,399 , GRCh38.p12 chr14: 23,629,190-23,629,190 DHRS2
    nsv3922265copy number variation1nstd102humanLikely pathogenic NCBI36 chr14: 19,950,586-24,557,166 , GRCh37 chr14: 20,880,746-25,487,326 , GRCh38 chr14: 20,412,587-25,018,120 ANG, APEX1, 346 more genes
    nsv3919106copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482 SRMP2, IGHV3-71, 1929 more genes
    nsv3918965copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,490,852-44,562,875 , GRCh38 chr14: 20,022,693-44,093,672 , NCBI36 chr14: 19,560,692-43,632,625 TRAJ13, LRP10, 589 more genes
    nsv3917422copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478 MIR656, TRAJ59, 1918 more genes
    nsv3917157copy number variation1nstd102humanPathogenic GRCh37 chr14: 24,018,169-42,452,605 , GRCh38 chr14: 23,548,960-41,983,402 , NCBI36 chr14: 23,088,009-41,522,355 LINC02300, COCH, 274 more genes
    nsv3916277copy number variation1nstd102humanPathogenic NCBI36 chr14: 19,734,944-44,823,755 , GRCh38 chr14: 20,196,945-45,284,802 , GRCh37 chr14: 20,665,104-45,754,005 MIR208B, MRPL52, 600 more genes
    nsv3913465copy number variation1nstd102humanUncertain significance GRCh38 chr14: 23,260,803-23,763,521 , GRCh37 chr14: 23,730,012-24,232,730 , NCBI36 chr14: 22,799,852-23,302,570 IL25, HMGN2P1, 27 more genes
    nsv3913204copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-49,111,245 , GRCh38 chr14: 20,043,513-48,642,042 , NCBI36 chr14: 19,581,512-48,180,995 SMARCE1P3, LOC100421646, 635 more genes
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