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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3906199copy number variation1nstd102humanBenign GRCh37 chr9: 140,087,121-140,094,212 , GRCh38.p12 chr9: 137,192,669-137,199,760 TPRN
    nsv3904570copy number variation1nstd102humanBenign GRCh37 chr9: 140,087,121-140,094,199 , GRCh38.p12 chr9: 137,192,669-137,199,747 TPRN
    nsv3902990copy number variation1nstd102humanBenign GRCh37 chr9: 140,088,574-140,094,273 , GRCh38.p12 chr9: 137,194,122-137,199,821 TPRN
    nsv3892643copy number variation1nstd102humanBenign GRCh37 chr9: 140,088,574-140,094,212 , GRCh38.p12 chr9: 137,194,122-137,199,760 TPRN
    nsv3908646copy number variation1nstd102humanBenign GRCh37 chr9: 140,093,188-140,094,212 , GRCh38.p12 chr9: 137,198,736-137,199,760 TPRN
    nsv3909393copy number variation1nstd102humanBenign GRCh37 chr9: 140,093,495-140,094,273 , GRCh38.p12 chr9: 137,199,043-137,199,821 TPRN
    nsv3906649copy number variation1nstd102humanBenign GRCh37 chr9: 140,093,495-140,094,212 , GRCh38.p12 chr9: 137,199,043-137,199,760 TPRN
    nsv3898971copy number variation1nstd102humanBenign GRCh37 chr9: 140,093,495-140,094,199 , GRCh38.p12 chr9: 137,199,043-137,199,747 TPRN
    nsv3906184copy number variation1nstd102humanBenign GRCh37 chr9: 140,093,531-140,094,212 , GRCh38.p12 chr9: 137,199,079-137,199,760 TPRN
    nsv3918779copy number variation1nstd102humanPathogenic GRCh37 chr9: 137,320,520-141,049,374 , NCBI36 chr9: 136,460,341-140,169,195 , GRCh38 chr9: 134,428,674-138,154,922 TPRN, LRRC26, 160 more genes
    nsv3891854copy number variation1nstd102humanPathogenic GRCh37 chr9: 137,816,459-141,114,095 , GRCh38.p12 chr9: 134,924,613-138,223,645 TPRN, LCN10, 147 more genes
    nsv3899903copy number variation1nstd102humanPathogenic GRCh37 chr9: 138,209,358-141,020,389 , GRCh38.p12 chr9: 135,317,512-138,125,937 TPRN, NSMF, 137 more genes
    nsv3896336copy number variation1nstd102humanPathogenic GRCh37 chr9: 138,222,049-141,018,925 , GRCh38.p12 chr9: 135,330,203-138,124,473 TPRN, LINC02907, 137 more genes
    nsv4685995copy number variation1nstd102humanPathogenic GRCh37 chr9: 138,225,001-141,015,001 , GRCh38.p12 chr9: 135,333,155-138,120,549 TPRN, CCDC183, 137 more genes
    nsv7098070copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr9: 138,392,557-141,016,451 , GRCh38.p12 chr9: 135,500,711-138,121,999 TPRN, STPG3-AS1, 132 more genes
    nsv7093414copy number variation1nstd102humanPathogenic GRCh38 chr9: 134,932,722-137,269,957 , GRCh37.p13 chr9: 137,824,568-140,164,409 TPRN, LHX3, 121 more genes
    nsv6313935copy number variation1nstd102humanPathogenic GRCh37 chr9: 138,740,078-141,020,389 , GRCh38.p12 chr9: 135,848,232-138,125,937 TPRN, ENTR1, 115 more genes
    nsv3922926copy number variation1nstd102humanPathogenic NCBI36 chr9: 137,483,683-139,628,011 , GRCh37 chr9: 138,343,862-140,508,190 , GRCh38 chr9: 135,452,016-137,613,738 TPRN, SSNA1, 126 more genes
    nsv4681206copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr9: 138,645,763-140,729,425 , GRCh38.p12 chr9: 135,753,917-137,834,973 TPRN, DPP7, 112 more genes
    nsv4768352copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,018,777-141,018,984 , GRCh38.p12 chr9: 136,126,931-138,124,532 TPRN, MIR6722, 108 more genes
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