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Items: 1 to 20 of 235

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074310inversion1nstd229human GRCh38 chr14: 22,076,285-27,854,954 , GRCh37.p13 chr14: 22,544,546-28,324,160 PPP1R3E, TRAJ37, 242 more genes
    nsv7061705inversion1nstd229human GRCh38 chr14: 22,453,373-22,611,174 , GRCh37.p13 chr14: 22,922,365-23,080,080 ABHD4, TRAJ55, 72 more genes
    nsv6939855copy number variation1nstd229human GRCh38 chr14: 22,512,398-22,580,943 , GRCh37.p13 chr14: 22,981,380-23,049,845 TRAJ10, TRAJ27, 33 more genes
    nsv6637318copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,690,196-23,114,522 , GRCh38.p12 chr14: 20,222,037-22,645,313 TRAJ21, TRAJ44, 239 more genes
    nsv6622466copy number variation1nstd224human GRCh37 chr14: 22,981,872-23,047,799 , GRCh38.p12 chr14: 22,512,890-22,578,899 TRAJ25, TRAJ22, 33 more genes
    nsv6486406copy number variation1nstd223human GRCh38 chr14: 21,538,051-22,772,225 , GRCh37.p13 chr14: 22,006,185-23,241,434 TRAJ54, TRAV9-1, 152 more genes
    nsv6315513copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-47,481,203 , GRCh38.p12 chr14: 20,043,513-47,012,000 CDH24, KLHL33, 623 more genes
    nsv6314715copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884 HNRNPC, FOXG1, 616 more genes
    nsv6290276copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 20,925,965-23,649,548 , GRCh38.p12 chr14: 20,457,806-23,180,339 ANG, APEX1, 255 more genes
    nsv6290029copy number variation1nstd218human GRCh38.p12 chr14: 21,973,760-22,547,657 , GRCh37 chr14: 22,441,989-23,016,598 , TRA, 108 more genes
    nsv6132775copy number variation1nstd213human GRCh37 chr14: 22,590,000-24,410,001 , GRCh38.p12 chr14: 22,122,042-23,940,792 BCL2L2, CEBPE, 167 more genes
    nsv5855295copy number variation1nstd209human GRCh38 chr14: 22,550,123-22,551,422 , GRCh37.p13 chr14: 23,019,067-23,020,367 TRAC, TRA
    nsv5503240copy number variation1nstd206human GRCh38 chr14: 22,548,641-22,548,711 , GRCh37.p13 chr14: 23,017,582-23,017,656 TRAC, TRA
    nsv5349028translocation1nstd200human GRCh38 chr14: 22,548,711-22,548,711 , GRCh38 chr14: 22,548,641-22,548,641 , GRCh37.p13 chr14: 23,017,656-23,017,656 , GRCh37.p13 chr14: 23,017,582-23,017,582 TRA, TRAC
    nsv5278812copy number variation1nstd204human GRCh38.p13 chr14: 21,896,901-22,636,500 , GRCh37.p13 chr14: 22,365,081-23,105,185 , TRAV23DV6, 119 more genes
    nsv4990804copy number variation1nstd200human GRCh38 chr14: 22,549,888-22,552,409 , GRCh37.p13 chr14: 23,018,832-23,021,352 TRA, TRAC
    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
    nsv4680172copy number variation1nstd189human GRCh37.p13 chr14: 22,893,640-23,020,319 , GRCh38.p12 chr14: 22,424,649-22,551,374 , TRA, 73 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
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