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Items: 1 to 20 of 238

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5917312copy number variation1nstd209human GRCh38 chr11: 95,207,140-95,209,978 , GRCh37.p13 chr11: 94,940,304-94,943,142 SESN3
    nsv5914215copy number variation1nstd209human GRCh38 chr11: 95,187,998-95,189,420 , GRCh37.p13 chr11: 94,921,162-94,922,584 SESN3
    nsv5849357copy number variation1nstd209human GRCh38 chr11: 95,207,188-95,209,830 , GRCh37.p13 chr11: 94,940,352-94,942,994 SESN3
    nsv5713145mobile element insertion2nstd211human GRCh38 chr11: 95,203,161-95,203,161 , GRCh37.p13 chr11: 94,936,325-94,936,325 SESN3
    nsv5711155mobile element insertion1nstd211human GRCh38 chr11: 95,220,332-95,220,332 , GRCh37.p13 chr11: 94,953,496-94,953,496 SESN3
    nsv5703316mobile element insertion1nstd211human GRCh38 chr11: 95,226,049-95,226,049 , GRCh37.p13 chr11: 94,959,213-94,959,213 SESN3
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5586976copy number variation1nstd207human GRCh38 chr11: 95,207,145-95,209,977 , GRCh37.p13 chr11: 94,940,309-94,943,141 SESN3
    nsv5505313copy number variation1nstd206human GRCh38 chr11: 95,196,935-95,197,013 , GRCh37.p13 chr11: 94,930,099-94,930,177 SESN3
    nsv5499529copy number variation1nstd206human GRCh38 chr11: 95,207,140-95,209,979 , GRCh37.p13 chr11: 94,940,304-94,943,143 SESN3
    nsv5499318copy number variation1nstd206human GRCh38 chr11: 95,187,958-95,189,461 , GRCh37.p13 chr11: 94,921,122-94,922,625 SESN3
    nsv5405545mobile element insertion1nstd206human GRCh38 chr11: 95,220,332-95,220,334 , GRCh37.p13 chr11: 94,953,496-94,953,498 SESN3
    nsv5397494mobile element insertion1nstd206human GRCh38 chr11: 95,203,161-95,203,212 , GRCh37.p13 chr11: 94,936,325-94,936,376 SESN3
    nsv5389629copy number variation2nstd186human GRCh37 chr11: 94,940,304-94,943,143 , GRCh38.p12 chr11: 95,207,140-95,209,979 SESN3
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5319461copy number variation1nstd204human GRCh38.p13 chr11: 95,207,138-95,209,981 , GRCh37.p13 chr11: 94,940,302-94,943,145 SESN3
    nsv5275393copy number variation1nstd204human GRCh38.p13 chr11: 95,207,101-95,210,000 , GRCh37.p13 chr11: 94,940,265-94,943,164 SESN3
    nsv5274222copy number variation1nstd204human GRCh38.p13 chr11: 95,206,488-95,208,664 , GRCh37.p13 chr11: 94,939,652-94,941,828 SESN3
    nsv5273168copy number variation1nstd204human GRCh38.p13 chr11: 95,206,888-95,210,280 , GRCh37.p13 chr11: 94,940,052-94,943,444 SESN3
    nsv5037979inversion1nstd200human GRCh38 chr11: 93,899,952-96,855,215 , GRCh37.p13 chr11: 93,633,118-96,726,215 , GPR83, 52 more genes
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