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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5936195copy number variation1nstd209human GRCh38 chr19: 53,715,842-53,763,296 , GRCh37.p13 chr19: 54,219,096-54,266,550 MIR521-1, MIR518A1, 24 more genes
    nsv5935137copy number variation1nstd209human GRCh38 chr19: 52,932,265-54,037,356 , GRCh37.p13 chr19: 53,435,518-54,528,887 LOC107987264, CACNG6, 113 more genes
    nsv5931914copy number variation1nstd209human GRCh38 chr19: 53,672,928-53,819,237 , GRCh37.p13 chr19: 54,176,182-54,322,491 MIR516B2, MIR520D, 56 more genes
    nsv5285078copy number variation1nstd204human GRCh38.p13 chr19: 53,719,866-53,720,865 , GRCh37.p13 chr19: 54,223,120-54,224,119 MIR520D, MIR517B, 1 more genes
    nsv5024894copy number variation1nstd200human GRCh38 chr19: 53,672,928-53,819,261 , GRCh37.p13 chr19: 54,176,182-54,322,515 MIR515-1, MIR1283-1, 56 more genes
    nsv5021267copy number variation1nstd200human GRCh38 chr19: 53,719,200-53,719,835 , GRCh37.p13 chr19: 54,222,454-54,223,089 MIR517B, RNU6-803P, 1 more genes
    nsv4853556copy number variation1nstd200human GRCh37 chr19: 54,222,453-54,223,089 , GRCh38.p12 chr19: 53,719,199-53,719,835 MIR517B, MIR520D, 1 more genes
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
    nsv4685764copy number variation1nstd102humannot provided GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460 SNAR-G1, IRF3, 453 more genes
    nsv4630282copy number variation1nstd183human GRCh37 chr19: 54,024,640-54,370,843 , GRCh38.p12 chr19: 53,521,386-53,867,589 MIR519A2, MIR518D, 70 more genes
    nsv4623997copy number variation1nstd183human GRCh37 chr19: 54,042,427-54,261,320 , GRCh38.p12 chr19: 53,539,173-53,758,066 RNU6-698P, MIR518A2, 56 more genes
    nsv4457565copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,214,278-54,321,973 , GRCh38.p12 chr19: 53,711,024-53,818,719 MIR521-1, MIR518A1, 36 more genes
    nsv4436464copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,039,784-54,484,439 , GRCh38 chr19: 53,536,530-53,981,185 MIR1283-2, MIR515-1, 74 more genes
    nsv4417845copy number variation1nstd174human GRCh37 chr19: 54,033,686-54,229,395 , GRCh38.p12 chr19: 53,530,432-53,726,141 MIR512-2, MIR515-1, 40 more genes
    nsv4378526copy number variation1nstd173human GRCh37 chr19: 54,175,131-54,318,410 , GRCh38.p12 chr19: 53,671,877-53,815,156 MIR516B2, MIR515-1, 57 more genes
    nsv4374902copy number variation1nstd173human GRCh37 chr19: 54,044,223-54,232,286 , GRCh38.p12 chr19: 53,540,969-53,729,032 MIR521-2, MIR520A, 42 more genes
    nsv4370999copy number variation1nstd173human GRCh37 chr19: 53,892,435-54,649,514 , GRCh38.p12 chr19: 53,389,182-54,071,460 ZNF765, MIR520D, 88 more genes
    nsv4366747copy number variation1nstd173human GRCh37 chr19: 53,888,553-54,626,548 , GRCh38.p12 chr19: 53,385,300-54,071,460 MIR522, MIR518F, 90 more genes
    nsv4268668copy number variation1nstd166human GRCh37.p13 chr19: 54,217,173-54,225,966 , GRCh38.p12 chr19: 53,713,919-53,722,712 MIR519D, MIR521-2, 4 more genes
    nsv4263576copy number variation1nstd166human GRCh37.p13 chr19: 54,222,473-54,223,035 , GRCh38.p12 chr19: 53,719,219-53,719,781 RNU6-803P, MIR520D, 1 more genes
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