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Items: 1 to 20 of 194

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148126copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,851,693-22,089,506 , GRCh38.p12 chr14: 21,383,534-21,621,353 OR10G3, SNORD9, 17 more genes
    nsv7138161copy number variation1nstd232human GRCh37.p13 chr14: 21,831,106-21,831,191 , GRCh38.p12 chr14: 21,362,947-21,363,032 SUPT16H
    nsv7094421copy number variation1nstd102humanUncertain significance GRCh37 chr14: 21,671,278-22,005,055 , GRCh38.p12 chr14: 21,203,119-21,536,921 RN7SL650P, SNORD9, 14 more genes
    nsv7094323copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,792,757-21,899,802 , GRCh38.p12 chr14: 21,324,598-21,431,643 UBA52P2, SUPT16H, 7 more genes
    nsv7094248copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 21,819,243-21,819,375 , GRCh38.p12 chr14: 21,351,084-21,351,216 SUPT16H, RPGRIP1
    nsv7094244copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,915,399-22,005,055 , GRCh38.p12 chr14: 20,447,240-21,536,921 ARHGEF40, LOC105370398, 78 more genes
    nsv7072621inversion1nstd229human GRCh38 chr14: 20,991,576-21,885,954 , GRCh37.p13 chr14: 21,459,735-22,354,136 LINC00641, TRAV13-1, 61 more genes
    nsv7071285inversion1nstd229human GRCh38 chr14: 21,372,717-21,372,728 , GRCh37.p13 chr14: 21,840,876-21,840,887 SUPT16H
    nsv7070409inversion1nstd229human GRCh38 chr14: 21,315,978-21,363,542 , GRCh37.p13 chr14: 21,784,137-21,831,701 RPGRIP1, SUPT16H
    nsv7059593inversion1nstd229human GRCh38 chr14: 21,238,320-21,375,314 , GRCh37.p13 chr14: 21,706,479-21,843,473 MRPS17P6, RPGRIP1, 2 more genes
    nsv6954715copy number variation1nstd229human GRCh38 chr14: 21,360,691-21,363,197 , GRCh37.p13 chr14: 21,828,850-21,831,356 SUPT16H
    nsv6948074copy number variation1nstd229human GRCh38 chr14: 21,381,027-21,382,644 , GRCh37.p13 chr14: 21,849,186-21,850,803 SUPT16H, LOC107984643
    nsv6946525copy number variation1nstd229human GRCh38 chr14: 21,317,744-21,408,181 , GRCh37.p13 chr14: 21,785,903-21,876,340 CHD8, RPGRIP1, 5 more genes
    nsv6946281copy number variation1nstd229human GRCh38 chr14: 21,355,389-21,356,637 , GRCh37.p13 chr14: 21,823,548-21,824,796 SUPT16H
    nsv6945924copy number variation1nstd229human GRCh38 chr14: 21,211,381-21,450,257 , GRCh37.p13 chr14: 21,679,540-21,918,416 EIF4EBP1P1, RPGRIP1, 9 more genes
    nsv6637860copy number variation1nstd102humanUncertain significance GRCh37 chr14: 21,496,133-21,962,265 , GRCh38.p12 chr14: 21,027,974-21,494,106 ARHGEF40, RN7SL650P, 28 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
    nsv6590618inversion1nstd223human GRCh38 chr14: 21,349,090-21,350,279 , GRCh37.p13 chr14: 21,817,249-21,818,438 RPGRIP1, SUPT16H
    nsv6585410inversion1nstd223human GRCh38 chr14: 21,349,357-21,350,397 , GRCh37.p13 chr14: 21,817,516-21,818,556 SUPT16H, RPGRIP1
    nsv6578229inversion1nstd223human GRCh38 chr14: 21,354,686-21,355,134 , GRCh37.p13 chr14: 21,822,845-21,823,293 SUPT16H
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