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Items: 1 to 20 of 266

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146234insertion1nstd232human GRCh37.p13 chr9: 135,253,991-135,253,991 , GRCh38.p12 chr9: 132,378,604-132,378,604 TTF1
    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
    nsv7098066copy number variation4nstd102humanUncertain significance GRCh37 chr9: 135,139,626-140,034,216 , GRCh38.p12 chr9: 132,264,239-137,139,764 LINC02692, SNORD141A, 181 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
    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
    nsv6878035copy number variation1nstd229human GRCh38 chr9: 132,367,730-132,375,710 , GRCh37.p13 chr9: 135,243,117-135,251,097 TTF1
    nsv6872149copy number variation1nstd229human GRCh38 chr9: 132,394,190-132,400,613 , GRCh37.p13 chr9: 135,269,577-135,276,000 TTF1
    nsv6865560copy number variation1nstd229human GRCh38 chr9: 132,104,707-132,425,204 , GRCh37.p13 chr9: 134,980,094-135,300,591 CFAP77, SETX, 5 more genes
    nsv6865080copy number variation1nstd229human GRCh38 chr9: 132,327,001-132,411,000 , GRCh37.p13 chr9: 135,202,388-135,286,387 SETX, LOC105376304, 2 more genes
    nsv6860454copy number variation1nstd229human GRCh38 chr9: 132,402,335-132,406,901 , GRCh37.p13 chr9: 135,277,722-135,282,288 TTF1
    nsv6574385inversion1nstd223human GRCh38 chr9: 132,396,719-132,397,718 , GRCh37.p13 chr9: 135,272,106-135,273,105 TTF1
    nsv6573395inversion1nstd223human GRCh38 chr9: 132,393,984-132,394,866 , GRCh37.p13 chr9: 135,269,371-135,270,253 TTF1
    nsv6559936inversion1nstd223human GRCh38 chr9: 132,400,586-132,401,171 , GRCh37.p13 chr9: 135,275,973-135,276,558 TTF1
    nsv6557067inversion1nstd223human GRCh38 chr9: 132,385,684-132,388,709 , GRCh37.p13 chr9: 135,261,071-135,264,096 TTF1
    nsv6556944inversion1nstd223human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 MIR4669, AK8, 196 more genes
    nsv6452469copy number variation1nstd223human GRCh38 chr9: 132,367,719-132,375,706 , GRCh37.p13 chr9: 135,243,106-135,251,093 TTF1
    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
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