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Items: 1 to 20 of 353

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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
    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
    nsv7016902copy number variation1nstd229human GRCh38 chr19: 3,678,651-3,686,526 , GRCh37.p13 chr19: 3,678,649-3,686,524 PIP5K1C
    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
    nsv7006877copy number variation1nstd229human GRCh38 chr19: 3,668,234-3,675,045 , GRCh37.p13 chr19: 3,668,232-3,675,043 PIP5K1C
    nsv7006155copy number variation1nstd229human GRCh38 chr19: 3,651,071-3,651,237 , GRCh37.p13 chr19: 3,651,069-3,651,235 PIP5K1C
    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
    nsv6998400copy number variation1nstd229human GRCh38 chr19: 3,687,801-3,694,500 , GRCh37.p13 chr19: 3,687,799-3,694,498 PIP5K1C
    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
    nsv6535348copy number variation1nstd223human GRCh38 chr19: 3,685,575-3,689,494 , GRCh37.p13 chr19: 3,685,573-3,689,492 PIP5K1C
    nsv6530592copy number variation1nstd223human GRCh38 chr19: 3,689,483-3,694,092 , GRCh37.p13 chr19: 3,689,481-3,694,090 PIP5K1C
    nsv6521260copy number variation1nstd223human GRCh38 chr19: 3,669,708-3,691,217 , GRCh37.p13 chr19: 3,669,706-3,691,215 PIP5K1C
    nsv6516719copy number variation1nstd223human GRCh38 chr19: 3,685,501-3,694,100 , GRCh37.p13 chr19: 3,685,499-3,694,098 PIP5K1C
    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
    nsv6283728copy number variation1nstd214human GRCh38 chr19: 3,697,046-3,697,215 , GRCh37.p13 chr19: 3,697,044-3,697,213 PIP5K1C
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