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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5535965copy number variation1nstd206human GRCh38 chr22: 37,692,336-37,692,849 , GRCh37.p13 chr22: 38,088,343-38,088,856 NOL12
    nsv5281012copy number variation1nstd204human GRCh38.p13 chr22: 37,662,501-37,724,300 , GRCh37.p13 chr22: 38,058,508-38,120,307 LGALS1, PDXP, 3 more genes
    nsv5038814copy number variation1nstd200human GRCh38 chr22: 37,683,535-37,687,543 , GRCh37.p13 chr22: 38,079,542-38,083,550 NOL12
    nsv5037692copy number variation1nstd200human GRCh38 chr22: 37,668,255-37,711,473 , GRCh37.p13 chr22: 38,064,262-38,107,480 LGALS1, TRIOBP, 2 more genes
    nsv4880622copy number variation1nstd200human GRCh37 chr22: 38,064,262-38,107,480 , GRCh38.p12 chr22: 37,668,255-37,711,473 RN7SL385P, TRIOBP, 2 more genes
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4676292copy number variation1nstd102humanPathogenic GRCh37 chr22: 30,654,764-51,197,838 , GRCh38.p12 chr22: 30,258,775-50,759,410 PDXP-DT, PDGFB, 550 more genes
    nsv4676116copy number variation1nstd102humanPathogenic GRCh37 chr22: 38,002,218-38,973,070 , GRCh38.p12 chr22: 37,606,211-38,577,065 CSNK1E, RN7SL704P, 43 more genes
    nsv4632242copy number variation1nstd183human GRCh37 chr22: 38,065,863-38,102,890 , GRCh38.p12 chr22: 37,669,856-37,706,883 TRIOBP, LGALS1, 2 more genes
    nsv4457771copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410 IGLV3-27, XKR3, 1082 more genes
    nsv4421543copy number variation1nstd174human GRCh37 chr22: 38,089,975-38,091,219 , GRCh38.p12 chr22: 37,693,968-37,695,212 TRIOBP, NOL12
    nsv4284730copy number variation1nstd166human GRCh37.p13 chr22: 38,087,415-38,087,680 , GRCh38.p12 chr22: 37,691,408-37,691,673 NOL12
    nsv4283475copy number variation1nstd166human GRCh37.p13 chr22: 38,080,000-38,092,500 , GRCh38.p12 chr22: 37,683,993-37,696,493 TRIOBP, NOL12
    nsv4278013copy number variation1nstd166human GRCh37.p13 chr22: 37,381,892-38,500,309 , GRCh38.p12 chr22: 36,985,851-38,104,302 GGA1, GALR3, 46 more genes
    nsv3922128copy number variation1nstd102humanPathogenic GRCh37 chr22: 35,729,986-39,296,182 , NCBI36 chr22: 34,059,986-37,626,128 , GRCh38 chr22: 35,333,993-38,900,177 LOC102724378, CARD10, 120 more genes
    nsv3919881copy number variation1nstd102humanPathogenic GRCh37 chr22: 17,397,633-51,178,213 , GRCh38 chr22: 16,916,743-50,739,785 , NCBI36 chr22: 15,777,633-49,525,079 MIR12114, MIR6820, 1059 more genes
    nsv3919085copy number variation1nstd102humanPathogenic NCBI36 chr22: 17,008,132-49,591,432 , GRCh37.p13 chr22: 18,628,132-51,244,566 , GRCh38.p12 chr22: 18,145,365-50,806,138 IGLV2-28, LINC01310, 1023 more genes
    nsv3915039copy number variation1nstd102humanPathogenic GRCh38 chr22: 37,447,222-39,103,680 , GRCh37 chr22: 37,843,259-39,499,685 , NCBI36 chr22: 36,173,205-37,829,631 MIR4534, SLC16A8, 68 more genes
    nsv3913775copy number variation1nstd102humanPathogenic NCBI36 chr22: 15,777,498-49,525,130 , GRCh38 chr22: 16,916,608-50,739,836 , GRCh37 chr22: 17,397,498-51,178,264 ZNF280A, RFPL1S, 1059 more genes
    nsv3913040copy number variation1nstd102humanUncertain significance NCBI36 chr22: 36,263,270-36,529,310 , GRCh38 chr22: 37,537,317-37,803,357 , GRCh37 chr22: 37,933,324-38,199,364 PDXP-DT, CDC42EP1, 10 more genes
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