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Items: 1 to 20 of 299

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124386copy number variation1nstd186human GRCh37 chr18: 51,831,868-51,832,052 , GRCh38.p12 chr18: 54,305,498-54,305,682 POLI
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5931132copy number variation1nstd209human GRCh38 chr18: 54,305,498-54,305,681 , GRCh37.p13 chr18: 51,831,868-51,832,051 POLI
    nsv5729166mobile element insertion2nstd211human GRCh38 chr18: 54,282,775-54,282,775 , GRCh37.p13 chr18: 51,809,145-51,809,145 POLI
    nsv5725430mobile element insertion1nstd211human GRCh38 chr18: 54,296,257-54,296,257 , GRCh37.p13 chr18: 51,822,627-51,822,627 POLI
    nsv5707349mobile element insertion2nstd211human GRCh38 chr18: 54,299,612-54,299,612 , GRCh37.p13 chr18: 51,825,982-51,825,982 POLI
    nsv5587978copy number variation1nstd207human GRCh38 chr18: 54,305,498-54,305,681 , GRCh37.p13 chr18: 51,831,868-51,832,051 POLI
    nsv5562338mobile element insertion1nstd206human GRCh38 chr18: 54,296,257-54,296,308 , GRCh37.p13 chr18: 51,822,627-51,822,678 POLI
    nsv5527226copy number variation1nstd206human GRCh38 chr18: 54,301,257-54,301,754 , GRCh37.p13 chr18: 51,827,627-51,828,124 POLI
    nsv5526337copy number variation1nstd206human GRCh38 chr18: 54,305,498-54,305,682 , GRCh37.p13 chr18: 51,831,868-51,832,052 POLI
    nsv5415960mobile element insertion1nstd206human GRCh38 chr18: 54,299,612-54,299,663 , GRCh37.p13 chr18: 51,825,982-51,826,033 POLI
    nsv5391109copy number variation1nstd186human GRCh37 chr18: 51,831,867-51,832,052 , GRCh38.p12 chr18: 54,305,497-54,305,682 POLI
    nsv5291310copy number variation1nstd204human GRCh38.p13 chr18: 54,305,501-54,305,700 , GRCh37.p13 chr18: 51,831,871-51,832,070 POLI
    nsv5018166copy number variation1nstd200human GRCh38 chr18: 54,320,506-54,334,268 , GRCh37.p13 chr18: 51,846,876-51,860,638 STARD6, POLI
    nsv5018165copy number variation1nstd200human GRCh38 chr18: 54,307,458-54,308,337 , GRCh37.p13 chr18: 51,833,828-51,834,707 POLI
    nsv4859685copy number variation1nstd200human GRCh37 chr18: 51,846,876-51,860,638 , GRCh38.p12 chr18: 54,320,506-54,334,268 STARD6, POLI
    nsv4859684copy number variation1nstd200human GRCh37 chr18: 51,831,840-51,832,079 , GRCh38.p12 chr18: 54,305,470-54,305,709 POLI
    nsv4733435copy number variation1nstd199human GRCh37 chr18: 51,831,866-51,832,050 , GRCh38.p12 chr18: 54,305,496-54,305,680 POLI
    nsv4676239copy number variation1nstd102humanUncertain significance GRCh37 chr18: 51,802,787-53,000,275 , GRCh38.p12 chr18: 54,276,417-55,333,044 RAB27B, CUPIN1P, 13 more genes
    nsv4676105copy number variation1nstd102humanPathogenic GRCh37 chr18: 49,460,596-78,014,123 , GRCh38.p12 chr18: 51,934,226-80,256,240 MIR548AV, GTSCR1, 310 more genes
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