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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6113876mobile element insertion1nstd186human GRCh37 chr15: 40,666,772-40,666,809 , GRCh38.p12 chr15: 40,374,571-40,374,608 DISP2
    nsv5968500insertion1nstd209human GRCh38 chr15: 40,374,556-40,374,556 , GRCh37.p13 chr15: 40,666,757-40,666,757 DISP2
    nsv5928387copy number variation1nstd209human GRCh38 chr15: 40,356,113-40,356,244 , GRCh37.p13 chr15: 40,648,314-40,648,445 DISP2, PHGR1
    nsv5719722mobile element insertion1nstd211human GRCh38 chr15: 40,355,519-40,355,519 , GRCh37.p13 chr15: 40,647,720-40,647,720 DISP2, PHGR1
    nsv5669729inversion1nstd207human GRCh38 chr15: 40,333,147-40,369,327 , GRCh37.p13 chr15: 40,625,348-40,661,528 DISP2, CCDC9B, 1 more genes
    nsv5663896insertion1nstd207human GRCh38 chr15: 40,374,014-40,374,014 , GRCh37.p13 chr15: 40,666,215-40,666,215 DISP2
    nsv5646037insertion1nstd207human GRCh38 chr15: 40,374,556-40,374,556 , GRCh37.p13 chr15: 40,666,757-40,666,757 DISP2
    nsv5602682copy number variation1nstd207human GRCh38 chr15: 40,356,113-40,356,178 , GRCh37.p13 chr15: 40,648,314-40,648,379 DISP2, PHGR1
    nsv5557547mobile element insertion1nstd206human GRCh38 chr15: 40,355,519-40,355,570 , GRCh37.p13 chr15: 40,647,720-40,647,771 DISP2, PHGR1
    nsv5513264copy number variation1nstd206human GRCh38 chr15: 40,377,106-40,378,863 , GRCh37.p13 chr15: 40,669,307-40,671,064 DISP2
    nsv5424813mobile element insertion1nstd206human GRCh38 chr15: 40,374,571-40,374,608 , GRCh37.p13 chr15: 40,666,772-40,666,809 DISP2
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5160004mobile element insertion1nstd203human GRCh38 chr15: 40,374,563-40,374,571 , GRCh37.p13 chr15: 40,666,764-40,666,772 DISP2
    nsv5158153mobile element insertion1nstd203human GRCh38 chr15: 40,374,562-40,374,571 , GRCh37.p13 chr15: 40,666,763-40,666,772 DISP2
    nsv5157251mobile element insertion1nstd203human GRCh38 chr15: 40,374,559-40,374,571 , GRCh37.p13 chr15: 40,666,760-40,666,772 DISP2
    nsv5155683mobile element insertion1nstd203human GRCh38 chr15: 40,374,289-40,374,289 , GRCh37.p13 chr15: 40,666,490-40,666,490 DISP2
    nsv5148656mobile element insertion1nstd203human GRCh38 chr15: 40,374,560-40,374,571 , GRCh37.p13 chr15: 40,666,761-40,666,772 DISP2
    nsv5148442mobile element insertion1nstd203human GRCh38 chr15: 40,374,555-40,374,571 , GRCh37.p13 chr15: 40,666,756-40,666,772 DISP2
    nsv5146496mobile element insertion1nstd203human GRCh38 chr15: 40,374,564-40,374,571 , GRCh37.p13 chr15: 40,666,765-40,666,772 DISP2
    nsv5144471mobile element insertion1nstd203human GRCh38 chr15: 40,373,960-40,374,015 , GRCh37.p13 chr15: 40,666,161-40,666,216 DISP2
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