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Items: 1 to 20 of 233

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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
    nsv7095649copy number variation1nstd102humanUncertain significance GRCh37 chr19: 3,585,596-3,607,681 , GRCh38.p12 chr19: 3,585,598-3,607,683 GIPC3, CACTIN-AS1, 1 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
    nsv7070316inversion1nstd229human GRCh38 chr19: 3,349,620-3,668,217 , GRCh37.p13 chr19: 3,349,618-3,668,215 PIP5K1C, LOC105372245, 12 more genes
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7065682inversion1nstd229human GRCh38 chr19: 3,282,406-3,593,791 , GRCh37.p13 chr19: 3,282,404-3,593,789 CELF5, NFIC, 11 more genes
    nsv7014210copy number variation1nstd229human GRCh38 chr19: 3,600,959-3,645,221 , GRCh37.p13 chr19: 3,600,957-3,645,219 CACTIN, CACTIN-AS1, 2 more genes
    nsv7013023copy number variation1nstd229human GRCh38 chr19: 3,595,601-3,599,600 , GRCh37.p13 chr19: 3,595,599-3,599,598 TBXA2R
    nsv7012797copy number variation1nstd229human GRCh38 chr19: 3,597,197-3,601,044 , GRCh37.p13 chr19: 3,597,195-3,601,042 TBXA2R
    nsv7009595copy number variation1nstd229human GRCh38 chr19: 3,584,633-3,595,131 , GRCh37.p13 chr19: 3,584,631-3,595,129 GIPC3, TBXA2R
    nsv7000736copy number variation1nstd229human GRCh38 chr19: 3,597,426-3,604,975 , GRCh37.p13 chr19: 3,597,424-3,604,973 TBXA2R
    nsv7000289copy number variation1nstd229human GRCh38 chr19: 3,593,801-3,668,200 , GRCh37.p13 chr19: 3,593,799-3,668,198 PIP5K1C, TBXA2R, 3 more genes
    nsv6624864copy number variation1nstd224human GRCh37 chr19: 3,586,471-4,217,207 , GRCh38.p12 chr19: 3,586,473-4,217,210 MAP2K2, ZFR2, 24 more genes
    nsv6624462copy number variation1nstd224human GRCh37 chr19: 3,542,792-3,698,333 , GRCh38.p12 chr19: 3,542,794-3,698,335 TBXA2R, HMG20B, 6 more genes
    nsv6597296inversion1nstd223human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , ALKBH7, 192 more genes
    nsv6524214copy number variation1nstd223human GRCh38 chr19: 3,584,751-3,602,880 , GRCh37.p13 chr19: 3,584,749-3,602,878 TBXA2R, GIPC3
    nsv6522969copy number variation1nstd223human GRCh38 chr19: 3,596,663-3,599,359 , GRCh37.p13 chr19: 3,596,661-3,599,357 TBXA2R
    nsv6291587copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,501,624-5,357,124 , GRCh38.p12 chr19: 3,501,626-5,357,113 RN7SL202P, EIF1P6, 67 more genes
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
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