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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068813inversion1nstd229human GRCh38 chr19: 56,872,783-57,542,535 , GRCh37.p13 chr19: 57,384,151-58,053,903 ZNF550, ZNF773, 25 more genes
    nsv7015314copy number variation1nstd229human GRCh38 chr19: 57,206,664-57,248,116 , GRCh37.p13 chr19: 57,718,032-57,759,484 ZNF805, AURKC, 1 more genes
    nsv6625051copy number variation1nstd224human GRCh37 chr19: 56,901,396-57,956,715 , GRCh38.p12 chr19: 56,390,027-57,445,347 AURKC, ZIM2, 42 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
    nsv5292903copy number variation1nstd204human GRCh38.p13 chr19: 57,172,601-57,751,900 , GRCh37.p13 chr19: 57,683,969-58,263,268 TPRG1LP1, ZNF805, 30 more genes
    nsv4676349copy number variation1nstd102humanUncertain significance GRCh37 chr19: 57,671,695-57,745,390 , GRCh38.p12 chr19: 57,160,327-57,234,022 DUXA, ZNF264, 2 more genes
    nsv4457735copy number variation1nstd102humanUncertain significance GRCh37 chr19: 57,737,113-57,771,792 , GRCh38.p12 chr19: 57,225,745-57,260,424 AURKC, ZNF805
    nsv4457599copy number variation1nstd102humanUncertain significance GRCh37 chr19: 57,590,808-57,745,390 , GRCh38.p12 chr19: 57,079,440-57,234,022 AURKC, ZIM3, 5 more genes
    nsv4457364copy number variation1nstd102humanUncertain significance GRCh37 chr19: 57,718,739-57,760,953 , GRCh38.p12 chr19: 57,207,371-57,249,585 AURKC, ZNF805, 1 more genes
    nsv4373618copy number variation1nstd173human GRCh37 chr19: 57,658,220-57,780,096 , GRCh38.p12 chr19: 57,146,852-57,268,728 ZNF264, ZNF805, 4 more genes
    nsv4265162copy number variation1nstd166human GRCh37.p13 chr19: 57,718,500-57,761,000 , GRCh38.p12 chr19: 57,207,132-57,249,632 ZNF264, ZNF805, 1 more genes
    nsv4263295copy number variation1nstd166human GRCh37.p13 chr19: 57,739,721-57,740,400 , GRCh38.p12 chr19: 57,228,353-57,229,032 AURKC
    nsv4256879copy number variation1nstd166human GRCh37.p13 chr19: 57,736,179-57,741,484 , GRCh38.p12 chr19: 57,224,811-57,230,116 AURKC
    nsv4253572copy number variation1nstd166human GRCh37.p13 chr19: 57,741,900-57,761,000 , GRCh38.p12 chr19: 57,230,532-57,249,632 ZNF805, AURKC
    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
    nsv3923613copy number variation1nstd102humanPathogenic GRCh38 chr19: 52,612,432-58,581,203 , GRCh37 chr19: 53,115,685-59,092,570 , NCBI36 chr19: 57,807,497-63,784,382 ZNF71-SMIM17, MIR518E, 393 more genes
    nsv3922599copy number variation1nstd102humanPathogenic GRCh38 chr19: 51,141,518-58,539,965 , NCBI36 chr19: 56,336,587-63,743,144 , GRCh37 chr19: 51,644,775-59,051,332 LOC100421130, A1BG-AS1, 475 more genes
    nsv3921078copy number variation1nstd102humanUncertain significance GRCh37 chr19: 57,678,918-57,748,194 , NCBI36 chr19: 62,370,730-62,440,006 , GRCh38 chr19: 57,167,550-57,236,826 AURKC, LOC100132009, 2 more genes
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