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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098718copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,206,913-3,771,740 , GRCh38.p12 chr19: 1,206,914-3,771,742 GIPC3, GNG7, 117 more genes
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 NCLN, RN7SL202P, 223 more genes
    nsv7095226copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-4,818,389 , GRCh38.p12 chr19: 589,946-4,818,377 ATP5F1D, LOC102723798, 204 more genes
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7007953copy number variation1nstd229human GRCh38 chr19: 3,197,910-3,200,558 , GRCh37.p13 chr19: 3,197,908-3,200,556 NCLN
    nsv7003844copy number variation1nstd229human GRCh38 chr19: 3,202,076-3,212,885 , GRCh37.p13 chr19: 3,202,074-3,212,883 NCLN
    nsv6597296inversion1nstd223human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , ALKBH7, 192 more genes
    nsv6519590copy number variation1nstd223human GRCh38 chr19: 3,197,916-3,251,361 , GRCh37.p13 chr19: 3,197,914-3,251,359 CELF5, NCLN
    nsv6288949insertion1nstd214human GRCh38 chr19: 3,193,168-3,193,168 , GRCh37.p13 chr19: 3,193,166-3,193,166 NCLN
    nsv6282729copy number variation1nstd214human GRCh38 chr19: 3,190,999-3,191,060 , GRCh37.p13 chr19: 3,190,997-3,191,058 NCLN
    nsv6231721insertion1nstd214human GRCh38 chr19: 3,193,130-3,193,130 , GRCh37.p13 chr19: 3,193,128-3,193,128 NCLN
    nsv6207141copy number variation1nstd214human GRCh38 chr19: 3,191,006-3,191,064 , GRCh37.p13 chr19: 3,191,004-3,191,062 NCLN
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133468copy number variation1nstd213human GRCh37 chr19: 2,040,000-7,300,001 , GRCh38.p12 chr19: 2,040,001-7,299,990 TLE5, AMH, 192 more genes
    nsv6129751insertion1nstd186human GRCh37 chr19: 3,193,116-3,193,132 , GRCh38.p12 chr19: 3,193,118-3,193,134 NCLN
    nsv6129165insertion1nstd186human GRCh37 chr19: 3,193,116-3,193,128 , GRCh38.p12 chr19: 3,193,118-3,193,130 NCLN
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
    nsv5942775copy number variation1nstd209human GRCh38 chr19: 2,865,023-7,153,898 , GRCh37.p13 chr19: 2,865,021-7,153,909 , GNA15-DT, 159 more genes
    nsv5931159copy number variation1nstd209human GRCh38 chr19: 3,193,130-3,193,197 , GRCh37.p13 chr19: 3,193,128-3,193,195 NCLN
    nsv5877877copy number variation1nstd209human GRCh38 chr19: 3,196,803-3,197,902 , GRCh37.p13 chr19: 3,196,801-3,197,900 NCLN
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