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Items: 1 to 20 of 232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5957315insertion1nstd209human GRCh38 chr10: 15,149,442-15,149,442 , GRCh37.p13 chr10: 15,191,441-15,191,441 NMT2
    nsv5926694copy number variation1nstd209human GRCh38 chr10: 15,168,478-15,168,730 , GRCh37.p13 chr10: 15,210,477-15,210,729 , NMT2
    nsv5708050mobile element insertion2nstd211human GRCh38 chr10: 15,127,570-15,127,570 , GRCh37.p13 chr10: 15,169,569-15,169,569 NMT2
    nsv5706873mobile element insertion2nstd211human GRCh38 chr10: 15,161,110-15,161,110 , GRCh37.p13 chr10: 15,203,109-15,203,109 NMT2
    nsv5640610insertion1nstd207human GRCh38 chr10: 15,149,038-15,149,038 , GRCh37.p13 chr10: 15,191,037-15,191,037 NMT2
    nsv5634780insertion1nstd207human GRCh38 chr10: 15,149,442-15,149,442 , GRCh37.p13 chr10: 15,191,441-15,191,441 NMT2
    nsv5543865insertion1nstd206human GRCh38 chr10: 15,149,442-15,149,442 , GRCh37.p13 chr10: 15,191,441-15,191,441 NMT2
    nsv5489449copy number variation1nstd206human GRCh38 chr10: 15,126,999-15,127,314 , GRCh37.p13 chr10: 15,168,998-15,169,313 NMT2
    nsv5485664copy number variation1nstd206human GRCh38 chr10: 15,121,057-15,124,163 , GRCh37.p13 chr10: 15,163,056-15,166,162 NMT2
    nsv5381768copy number variation1nstd102humanPathogenic GRCh37 chr10: 9,137,489-17,227,168 , GRCh38.p12 chr10: 9,095,526-17,185,169 PROSER2, C1QL3, 110 more genes
    nsv5251980copy number variation1nstd204human GRCh38.p13 chr10: 15,118,534-15,120,033 , GRCh37.p13 chr10: 15,160,533-15,162,032 LOC105376431, NMT2
    nsv5248647copy number variation1nstd204human GRCh38.p13 chr10: 15,160,433-15,164,531 , GRCh37.p13 chr10: 15,202,432-15,206,530 NMT2
    nsv5131256mobile element insertion1nstd203human GRCh38 chr10: 15,127,546-15,127,570 , GRCh37.p13 chr10: 15,169,545-15,169,569 NMT2
    nsv5130612mobile element insertion1nstd203human GRCh38 chr10: 15,147,095-15,147,135 , GRCh37.p13 chr10: 15,189,094-15,189,134 NMT2
    nsv5129380mobile element insertion1nstd203human GRCh38 chr10: 15,127,529-15,127,587 , GRCh37.p13 chr10: 15,169,528-15,169,586 NMT2
    nsv5129066mobile element insertion1nstd203human GRCh38 chr10: 15,127,587-15,127,608 , GRCh37.p13 chr10: 15,169,586-15,169,607 NMT2
    nsv5126968mobile element insertion1nstd203human GRCh38 chr10: 15,127,524-15,127,587 , GRCh37.p13 chr10: 15,169,523-15,169,586 NMT2
    nsv5125182mobile element insertion1nstd203human GRCh38 chr10: 15,127,501-15,127,587 , GRCh37.p13 chr10: 15,169,500-15,169,586 NMT2
    nsv5124593mobile element insertion1nstd203human GRCh38 chr10: 15,127,578-15,127,587 , GRCh37.p13 chr10: 15,169,577-15,169,586 NMT2
    nsv5123043mobile element insertion1nstd203human GRCh38 chr10: 15,127,570-15,127,587 , GRCh37.p13 chr10: 15,169,569-15,169,586 NMT2
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