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Items: 1 to 20 of 105

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7058341inversion1nstd229human GRCh38 chr19: 57,867,886-58,461,146 , GRCh37.p13 chr19: 58,379,254-58,972,513 ZNF417, LETM1P2, 45 more genes
    nsv7017449copy number variation1nstd229human GRCh38 chr19: 58,292,208-58,414,659 , GRCh37.p13 chr19: 58,803,574-58,926,026 MIR10394, A1BG-AS1, 19 more genes
    nsv7012921copy number variation1nstd229human GRCh38 chr19: 58,325,544-58,426,849 , GRCh37.p13 chr19: 58,836,910-58,938,216 ZNF584, MIR6806, 15 more genes
    nsv7007574copy number variation1nstd229human GRCh38 chr19: 58,388,246-58,392,972 , GRCh37.p13 chr19: 58,899,613-58,904,339 MIR10394, RPS5
    nsv7002798copy number variation1nstd229human GRCh38 chr19: 58,379,248-58,406,273 , GRCh37.p13 chr19: 58,890,615-58,917,640 MIR10394, LINC02560, 6 more genes
    nsv7000299copy number variation1nstd229human GRCh38 chr19: 58,379,392-58,443,656 , GRCh37.p13 chr19: 58,890,759-58,955,023 RNF225, ZNF837, 8 more genes
    nsv6597711inversion1nstd223human GRCh38 chr19: 55,930,883-58,410,519 , GRCh37.p13 chr19: 56,442,249-58,921,886 ZNF667-AS1, ZNF606-AS1, 130 more genes
    nsv6597167inversion1nstd223human GRCh38 chr19: 55,930,699-58,410,630 , GRCh37.p13 chr19: 56,442,065-58,921,997 VN2R19P, RPL19P19, 130 more genes
    nsv6133477copy number variation1nstd213human GRCh37 chr19: 57,800,000-59,128,983 , GRCh38.p12 chr19: 57,288,632-58,607,616 A1BG, FKBP1AP1, 95 more genes
    nsv6133413copy number variation1nstd213human GRCh37 chr19: 57,870,000-59,128,983 , GRCh38.p12 chr19: 57,358,632-58,607,616 ZNF8, ZNF211, 92 more genes
    nsv5280745copy number variation1nstd204human GRCh38.p13 chr19: 57,881,401-58,501,600 , GRCh37.p13 chr19: 58,392,769-59,012,967 ZNF417, LOC112268251, 51 more genes
    nsv5172309mobile element insertion1nstd203human GRCh38 chr19: 58,392,142-58,392,154 , GRCh37.p13 chr19: 58,903,509-58,903,521 RPS5, MIR10394
    nsv4729813copy number variation1nstd102humanUncertain significance GRCh37 chr19: 58,687,912-58,946,147 , GRCh38.p12 chr19: 58,176,545-58,434,780 ZNF837, LOC100419840, 26 more genes
    nsv4622011copy number variation1nstd183human GRCh37 chr19: 58,843,539-58,937,748 , GRCh38.p12 chr19: 58,332,173-58,426,381 ZNF584, ZNF497-AS1, 14 more genes
    nsv4457575copy number variation1nstd102humanUncertain significance GRCh37 chr19: 58,882,821-58,995,308 , GRCh38.p12 chr19: 58,371,454-58,483,941 LINC02560, RNU6-1337P, 13 more genes
    nsv4387981copy number variation1nstd173human GRCh37 chr19: 58,791,335-58,956,888 , GRCh38.p12 chr19: 58,279,969-58,445,521 MIR6806, ZNF584, 21 more genes
    nsv4366940copy number variation1nstd173human GRCh37 chr19: 58,791,213-58,956,888 , GRCh38.p12 chr19: 58,279,847-58,445,521 LOC100419848, A1BG-AS1, 21 more genes
    nsv4261084copy number variation1nstd166human GRCh37.p13 chr19: 58,902,000-59,118,900 , GRCh38.p12 chr19: 58,390,633-58,607,533 , ZNF324B, 25 more genes
    nsv3924732copy number variation1nstd102humanPathogenic GRCh38 chr19: 49,907,832-58,557,889 , GRCh37 chr19: 50,411,089-59,069,256 , NCBI36 chr19: 55,102,901-63,761,068 RPL39P37, CCDC106, 556 more genes
    nsv3923909copy number variation1nstd102humanPathogenic NCBI36 chr19: 55,347,589-63,784,382 , GRCh37 chr19: 50,655,777-59,092,570 , GRCh38 chr19: 50,152,520-58,581,203 OSCAR, FKBP1AP1, 535 more genes
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