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Items: 1 to 20 of 479

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966753insertion1nstd209human GRCh38 chr2: 209,787,157-209,787,157 , GRCh37.p13 chr2: 210,651,881-210,651,881 UNC80
    nsv5959077insertion1nstd209human GRCh38 chr2: 209,844,442-209,844,442 , GRCh37.p13 chr2: 210,709,166-210,709,166 UNC80
    nsv5906028copy number variation1nstd209human GRCh38 chr2: 209,832,676-209,833,786 , GRCh37.p13 chr2: 210,697,400-210,698,510 UNC80
    nsv5893907copy number variation1nstd209human GRCh38 chr2: 209,925,674-209,925,739 , GRCh37.p13 chr2: 210,790,398-210,790,463 UNC80
    nsv5892279copy number variation1nstd209human GRCh38 chr2: 209,978,219-209,978,438 , GRCh37.p13 chr2: 210,842,943-210,843,162 UNC80
    nsv5832708copy number variation1nstd209human GRCh38 chr2: 209,832,659-209,833,808 , GRCh37.p13 chr2: 210,697,383-210,698,532 UNC80
    nsv5729535mobile element insertion1nstd211human GRCh38 chr2: 209,931,489-209,931,489 , GRCh37.p13 chr2: 210,796,213-210,796,213 UNC80
    nsv5693048mobile element insertion1nstd211human GRCh38 chr2: 209,776,069-209,776,069 , GRCh37.p13 chr2: 210,640,793-210,640,793 UNC80
    nsv5686464mobile element insertion2nstd211human GRCh38 chr2: 209,854,247-209,854,247 , GRCh37.p13 chr2: 210,718,971-210,718,971 UNC80
    nsv5684083mobile element insertion1nstd211human GRCh38 chr2: 209,872,389-209,872,389 , GRCh37.p13 chr2: 210,737,113-210,737,113 UNC80
    nsv5677861mobile element insertion2nstd211human GRCh38 chr2: 209,915,125-209,915,125 , GRCh37.p13 chr2: 210,779,849-210,779,849 UNC80
    nsv5623995insertion2nstd207human GRCh38 chr2: 209,903,521-209,903,521 , GRCh37.p13 chr2: 210,768,245-210,768,245 UNC80
    nsv5623930insertion1nstd207human GRCh38 chr2: 209,787,157-209,787,157 , GRCh37.p13 chr2: 210,651,881-210,651,881 UNC80
    nsv5612160insertion1nstd207human GRCh38 chr2: 209,956,305-209,956,305 , GRCh37.p13 chr2: 210,821,029-210,821,029 UNC80
    nsv5607466insertion1nstd207human GRCh38 chr2: 209,844,446-209,844,446 , GRCh37.p13 chr2: 210,709,170-210,709,170 UNC80
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5543469insertion1nstd206human GRCh38 chr2: 209,854,247-209,854,298 , GRCh37.p13 chr2: 210,718,971-210,719,022 UNC80
    nsv5537278insertion1nstd206human GRCh38 chr2: 209,915,111-209,915,111 , GRCh37.p13 chr2: 210,779,835-210,779,835 UNC80
    nsv5448970copy number variation1nstd206human GRCh38 chr2: 209,882,594-209,893,256 , GRCh37.p13 chr2: 210,747,318-210,757,980 UNC80
    nsv5448655copy number variation1nstd206human GRCh38 chr2: 209,868,912-209,871,060 , GRCh37.p13 chr2: 210,733,636-210,735,784 UNC80
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