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Items: 1 to 20 of 145

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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
    nsv7062185inversion1nstd229human GRCh38 chr9: 131,448,265-131,541,583 , GRCh37.p13 chr9: 134,323,652-134,416,970 UCK1, POMT1, 4 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
    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
    nsv6864589copy number variation1nstd229human GRCh38 chr9: 131,302,727-131,623,767 , GRCh37.p13 chr9: 134,178,114-134,499,154 LOC105376299, SNORD62A, 9 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
    nsv6574375inversion1nstd223human GRCh38 chr9: 131,365,326-131,500,133 , GRCh37.p13 chr9: 134,240,713-134,375,520 SNORD62A, PRRC2B, 2 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
    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
    nsv6439290copy number variation1nstd223human GRCh38 chr9: 131,471,992-131,563,559 , GRCh37.p13 chr9: 134,347,379-134,438,946 POMT1, SNORD62A, 5 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
    nsv6141958copy number variation1nstd206human GRCh38 chr9: 131,414,000-131,576,552 , GRCh37.p13 chr9: 134,289,387-134,451,939 , RAPGEF1, 7 more genes
    nsv6137445copy number variation1nstd213human GRCh37 chr9: 133,220,000-134,800,001 , GRCh38.p12 chr9: 130,347,674-131,924,614 ABL1, ASS1, 32 more genes
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