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Items: 1 to 20 of 210

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098427copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,857,676-135,942,612 , GRCh38.p12 chr9: 129,095,397-133,067,225 ASS1, SETX, 86 more genes
    nsv7097932copy number variation1nstd102humanUncertain significance GRCh37 chr9: 133,884,602-135,942,612 , GRCh38.p12 chr9: 131,009,215-133,067,225 LAMC3, SPACA9, 40 more genes
    nsv7097690copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,087,402-141,016,451 , GRCh38.p12 chr9: 128,325,123-138,121,999 REXO4, TOR1B, 324 more genes
    nsv7076868inversion1nstd229human GRCh38 chr9: 131,266,802-131,706,679 , GRCh37.p13 chr9: 134,142,189-134,582,066 LOC105376301, PRRT1B, 10 more genes
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv7075196inversion1nstd229human GRCh38 chr9: 130,990,409-137,053,229 , GRCh37.p13 chr9: 133,865,796-139,947,681 LINC02907, LCN1, 196 more genes
    nsv7059760inversion1nstd229human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 LCN10, RAPGEF1, 196 more genes
    nsv6874569copy number variation1nstd229human GRCh38 chr9: 131,262,038-131,262,971 , GRCh37.p13 chr9: 134,137,425-134,138,358 FAM78A
    nsv6869722copy number variation1nstd229human GRCh38 chr9: 131,014,600-131,315,332 , GRCh37.p13 chr9: 133,889,987-134,190,719 FAM78A, AIF1L, 4 more genes
    nsv6869056copy number variation1nstd229human GRCh38 chr9: 131,228,357-131,624,747 , GRCh37.p13 chr9: 134,103,744-134,500,134 POMT1, UCK1, 11 more genes
    nsv6867232copy number variation1nstd229human GRCh38 chr9: 130,826,301-131,964,500 , GRCh37.p13 chr9: 133,701,688-134,839,887 SNORD62A, FAM78A, 21 more genes
    nsv6859435copy number variation1nstd229human GRCh38 chr9: 131,220,301-131,964,500 , GRCh37.p13 chr9: 134,095,688-134,839,887 LOC105376300, NUP214, 14 more genes
    nsv6633668copy number variation1nstd224human GRCh37 chr9: 133,932,442-134,233,268 , GRCh38.p12 chr9: 131,057,055-131,357,881 NUP214, LAMC3, 6 more genes
    nsv6556944inversion1nstd223human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 MIR4669, AK8, 196 more genes
    nsv6452701copy number variation1nstd223human GRCh38 chr9: 131,258,676-131,259,010 , GRCh37.p13 chr9: 134,134,063-134,134,397 FAM78A
    nsv6450427copy number variation1nstd223human GRCh38 chr9: 131,262,017-131,263,150 , GRCh37.p13 chr9: 134,137,404-134,138,537 FAM78A
    nsv6442278copy number variation1nstd223human GRCh38 chr9: 131,225,001-132,519,900 , GRCh37.p13 chr9: 134,100,388-135,395,287 FAM78A, LOC105376302, 21 more genes
    nsv6437052copy number variation1nstd223human GRCh38 chr9: 131,240,901-131,472,900 , GRCh37.p13 chr9: 134,116,288-134,348,287 PLPP7, LOC105376300, 3 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6312756copy number variation1nstd102humanUncertain significance GRCh37 chr9: 133,901,652-134,398,493 , GRCh38.p12 chr9: 131,026,265-131,523,106 LOC105376299, SNORD62A, 12 more genes
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