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Items: 1 to 20 of 583

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960176insertion1nstd209human GRCh38 chr2: 111,964,043-111,964,043 , GRCh37.p13 chr2: 112,721,620-112,721,620 MERTK
    nsv5959995insertion1nstd209human GRCh38 chr2: 111,958,965-111,958,965 , GRCh37.p13 chr2: 112,716,542-112,716,542 MERTK
    nsv5886475copy number variation1nstd209human GRCh38 chr2: 111,960,326-111,961,790 , GRCh37.p13 chr2: 112,717,903-112,719,367 MERTK
    nsv5877037copy number variation1nstd209human GRCh38 chr2: 111,989,607-111,991,477 , GRCh37.p13 chr2: 112,747,184-112,749,054 MERTK
    nsv5870268copy number variation1nstd209human GRCh38 chr2: 112,006,207-112,007,764 , GRCh37.p13 chr2: 112,763,784-112,765,341 MERTK
    nsv5831177copy number variation1nstd209human GRCh38 chr2: 112,006,162-112,007,761 , GRCh37.p13 chr2: 112,763,739-112,765,338 MERTK
    nsv5831176copy number variation1nstd209human GRCh38 chr2: 111,960,388-111,961,792 , GRCh37.p13 chr2: 112,717,965-112,719,369 MERTK
    nsv5730222mobile element insertion1nstd211human GRCh38 chr2: 111,993,558-111,993,558 , GRCh37.p13 chr2: 112,751,135-112,751,135 MERTK
    nsv5729948mobile element insertion1nstd211human GRCh38 chr2: 111,930,675-111,930,675 , GRCh37.p13 chr2: 112,688,252-112,688,252 MERTK, RN7SL297P
    nsv5724670mobile element insertion1nstd211human GRCh38 chr2: 112,018,227-112,018,227 , GRCh37.p13 chr2: 112,775,804-112,775,804 MERTK
    nsv5723519mobile element insertion1nstd211human GRCh38 chr2: 111,902,199-111,902,199 , GRCh37.p13 chr2: 112,659,776-112,659,776 MERTK
    nsv5717607mobile element insertion2nstd211human GRCh38 chr2: 111,913,311-111,913,311 , GRCh37.p13 chr2: 112,670,888-112,670,888 MERTK
    nsv5717342mobile element insertion1nstd211human GRCh38 chr2: 111,902,214-111,902,214 , GRCh37.p13 chr2: 112,659,791-112,659,791 MERTK
    nsv5682946mobile element insertion2nstd211human GRCh38 chr2: 111,958,981-111,958,981 , GRCh37.p13 chr2: 112,716,558-112,716,558 MERTK
    nsv5677737mobile element insertion1nstd211human GRCh38 chr2: 112,020,429-112,020,429 , GRCh37.p13 chr2: 112,778,006-112,778,006 MERTK
    nsv5673450copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 112,760,649-112,767,663 , GRCh38.p12 chr2: 112,003,072-112,010,086 MERTK
    nsv5673449copy number variation1nstd102humanPathogenic GRCh37 chr2: 112,751,828-112,753,086 , GRCh38.p12 chr2: 111,994,251-111,995,509 MERTK
    nsv5673371copy number variation1nstd102humanPathogenic GRCh37 chr2: 112,702,517-112,786,441 , GRCh38.p12 chr2: 111,944,940-112,028,864 SLC30A6P1, MERTK
    nsv5673370copy number variation1nstd102humanPathogenic GRCh37 chr2: 112,656,313-112,733,049 , GRCh38.p12 chr2: 111,898,736-111,975,472 MERTK, RTRAFP1, 2 more genes
    nsv5621796insertion2nstd207human GRCh38 chr2: 111,944,498-111,944,498 , GRCh37.p13 chr2: 112,702,075-112,702,075 MERTK
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