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Items: 1 to 20 of 79

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5503475copy number variation1nstd206human GRCh38 chr14: 21,601,713-21,634,637 , GRCh37.p13 chr14: 22,069,863-22,102,793 OR10G2, TRAV1-1, 3 more genes
    nsv4728411copy number variation1nstd102humanUncertain significance GRCh37 chr14: 22,006,109-23,241,448 , GRCh38.p12 chr14: 21,537,975-22,772,239 OR4E2, TRAV10, 152 more genes
    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
    nsv4676085copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,143,933-23,297,667 , GRCh38.p12 chr14: 20,675,774-22,828,458 ANG, SNORD8, 209 more genes
    nsv4675977copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 21,159,605-22,252,320 , GRCh38.p12 chr14: 20,691,446-21,784,103 ANG, HNRNPC, 69 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
    nsv4628286copy number variation1nstd183human GRCh37 chr14: 22,071,202-22,104,306 , GRCh38.p12 chr14: 21,603,051-21,636,150 TRA, OR10G2, 3 more genes
    nsv4578270copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 21,717,093-24,027,220 , GRCh38.p12 chr14: 21,248,934-23,558,011 BCL2L2, CEBPE, 215 more genes
    nsv4455618copy number variation1nstd102humanUncertain significance GRCh37 chr14: 21,678,344-22,299,981 , GRCh38.p12 chr14: 21,210,185-21,831,825 TRAV3, RBBP4P5, 36 more genes
    nsv4426506copy number variation1nstd174human GRCh37 chr14: 22,070,046-22,102,835 , GRCh38.p12 chr14: 21,601,896-21,634,679 OR10G1P, TRAV1-1, 3 more genes
    nsv4365363copy number variation1nstd173human GRCh37 chr14: 22,033,010-22,562,282 , GRCh38.p12 chr14: 21,564,879-22,094,005 , TRAV5, 44 more genes
    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
    nsv4223209copy number variation1nstd166human GRCh37.p13 chr14: 22,095,569-22,713,973 , GRCh38.p12 chr14: 21,627,416-22,246,089 , TRAV8-5, 54 more genes
    nsv4218406copy number variation1nstd166human GRCh37.p13 chr14: 22,102,459-22,106,503 , GRCh38.p12 chr14: 21,634,303-21,638,273 TRA, OR10G2
    nsv3969812copy number variation1nstd168human GRCh38 chr14: 21,455,498-21,665,382 , GRCh37.p13 chr14: 21,923,657-22,133,596 TOX4, OR4E2, 14 more genes
    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
    nsv3920885copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,619,308-23,911,404 , NCBI36 chr14: 19,689,148-22,981,244 , GRCh38 chr14: 20,151,149-23,442,195 SLC39A2, APEX1, 294 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
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