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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141616copy number variation1nstd232human GRCh37.p13 chr19: 3,983,015-3,983,105 , GRCh38.p12 chr19: 3,983,017-3,983,107 EEF2, SNORD37
    nsv7141020copy number variation1nstd232human GRCh37.p13 chr19: 3,980,706-3,980,836 , GRCh38.p12 chr19: 3,980,708-3,980,838 EEF2, SNORD37
    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
    nsv7060352inversion1nstd229human GRCh38 chr19: 3,851,263-4,364,229 , GRCh37.p13 chr19: 3,851,261-4,364,226 DAPK3, YJU2, 22 more genes
    nsv7013041copy number variation1nstd229human GRCh38 chr19: 3,981,570-3,981,622 , GRCh37.p13 chr19: 3,981,568-3,981,620 SNORD37, EEF2
    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
    nsv6597296inversion1nstd223human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , ALKBH7, 192 more genes
    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
    nsv6291467copy number variation1nstd102humanUncertain significance GRCh37 chr19: 3,788,725-4,225,547 , GRCh38.p12 chr19: 3,788,727-4,225,550 ZFR2, SNORD37, 14 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
    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
    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
    nsv5381793copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,976,203-4,345,430 , GRCh38.p12 chr19: 3,976,205-4,345,433 MPND, SNORD37, 13 more genes
    nsv5294246copy number variation1nstd204human GRCh38.p13 chr19: 3,976,901-3,990,900 , GRCh37.p13 chr19: 3,976,899-3,990,898 SNORD37, EEF2
    nsv5293117copy number variation1nstd204human GRCh37.p13 chr19: 3,937,199-4,064,698 , GRCh38.p13 chr19: 3,937,201-4,064,700 DAPK3, EEF2, 5 more genes
    nsv5292408copy number variation1nstd204human GRCh38.p13 chr19: 2,552,101-4,875,100 , GRCh37.p13 chr19: 2,552,099-4,875,112 , S1PR4, 93 more genes
    nsv5290959copy number variation1nstd204human GRCh38.p13 chr19: 3,885,401-4,190,300 , GRCh37.p13 chr19: 3,885,399-4,190,297 PIAS4, ANKRD24, 11 more genes
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