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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6118147copy number variation1nstd186human GRCh37 chr2: 233,197,878-233,197,973 , GRCh38.p12 chr2: 232,333,168-232,333,263 DIS3L2
    nsv5950509insertion1nstd209human GRCh38 chr2: 232,086,659-232,086,659 , GRCh37.p13 chr2: 232,951,369-232,951,369 DIS3L2
    nsv5949209insertion1nstd209human GRCh38 chr2: 232,246,909-232,246,909 , GRCh37.p13 chr2: 233,111,619-233,111,619 DIS3L2
    nsv5899353copy number variation1nstd209human GRCh38 chr2: 232,326,575-232,440,030 , GRCh37.p13 chr2: 233,191,285-233,304,740 , ALPP, 6 more genes
    nsv5890881copy number variation1nstd209human GRCh38 chr2: 232,057,194-232,063,565 , GRCh37.p13 chr2: 232,921,904-232,928,275 DIS3L2
    nsv5832810copy number variation1nstd209human GRCh38 chr2: 232,057,130-232,063,168 , GRCh37.p13 chr2: 232,921,840-232,927,878 DIS3L2
    nsv5715973mobile element insertion1nstd211human GRCh38 chr2: 232,100,507-232,100,507 , GRCh37.p13 chr2: 232,965,217-232,965,217 DIS3L2
    nsv5692373mobile element insertion1nstd211human GRCh38 chr2: 232,046,836-232,046,836 , GRCh37.p13 chr2: 232,911,546-232,911,546 DIS3L2
    nsv5673695copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,001,172-233,075,125 , GRCh38.p12 chr2: 232,136,462-232,210,415 MIR562, DIS3L2
    nsv5673614copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,028,159-233,028,352 , GRCh38.p12 chr2: 232,163,449-232,163,642 DIS3L2
    nsv5610653insertion1nstd207human GRCh38 chr2: 232,246,907-232,246,907 , GRCh37.p13 chr2: 233,111,617-233,111,617 DIS3L2
    nsv5607752insertion1nstd207human GRCh38 chr2: 232,086,659-232,086,659 , GRCh37.p13 chr2: 232,951,369-232,951,369 DIS3L2
    nsv5605995insertion1nstd207human GRCh38 chr2: 232,086,171-232,086,171 , GRCh37.p13 chr2: 232,950,881-232,950,881 DIS3L2
    nsv5564690copy number variation1nstd207human GRCh38 chr2: 232,333,149-232,333,235 , GRCh37.p13 chr2: 233,197,859-233,197,945 DIS3L2
    nsv5564428copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr2: 232,879,638-232,952,441 , GRCh38.p12 chr2: 232,014,928-232,087,731 DIS3L2
    nsv5451826copy number variation1nstd206human GRCh38 chr2: 232,153,618-232,177,618 , GRCh37.p13 chr2: 233,018,328-233,042,328 DIS3L2, MIR562
    nsv5450691copy number variation1nstd206human GRCh38 chr2: 231,979,353-231,983,114 , GRCh37.p13 chr2: 232,844,063-232,847,824 DIS3L2
    nsv5450458copy number variation1nstd206human GRCh38 chr2: 232,226,924-232,227,048 , GRCh37.p13 chr2: 233,091,634-233,091,758 DIS3L2
    nsv5448892copy number variation1nstd206human GRCh38 chr2: 231,948,538-231,960,133 , GRCh37.p13 chr2: 232,813,248-232,824,843 DIS3L2
    nsv5447744copy number variation1nstd206human GRCh38 chr2: 231,984,888-231,992,541 , GRCh37.p13 chr2: 232,849,598-232,857,251 DIS3L2
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