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Items: 1 to 20 of 543

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124585insertion1nstd186human GRCh37 chr4: 75,068,934-75,068,968 , GRCh38.p12 chr4: 74,203,217-74,203,251 MTHFD2L
    nsv5980334inversion1nstd209human GRCh38 chr4: 74,213,878-74,222,235 , GRCh37.p13 chr4: 75,079,595-75,087,952 MTHFD2L
    nsv5969002inversion1nstd209human GRCh38 chr4: 74,221,828-74,225,834 , GRCh37.p13 chr4: 75,087,545-75,091,551 MTHFD2L
    nsv5966129insertion1nstd209human GRCh38 chr4: 74,291,003-74,291,003 , GRCh37.p13 chr4: 75,156,720-75,156,720 MTHFD2L, LOC105377276
    nsv5964999insertion1nstd209human GRCh38 chr4: 74,188,742-74,188,742 , GRCh37.p13 chr4: 75,054,459-75,054,459 MTHFD2L
    nsv5903695copy number variation1nstd209human GRCh38 chr4: 74,148,633-74,149,493 , GRCh37.p13 chr4: 75,014,350-75,015,210 MTHFD2L
    nsv5893576copy number variation1nstd209human GRCh38 chr4: 67,920,462-75,134,545 , GRCh37.p13 chr4: 68,786,180-76,059,755 , DCK, 147 more genes
    nsv5840380copy number variation1nstd209human GRCh38 chr4: 74,213,850-74,217,849 , GRCh37.p13 chr4: 75,079,567-75,083,566 MTHFD2L
    nsv5728703mobile element insertion1nstd211human GRCh38 chr4: 74,185,170-74,185,170 , GRCh37.p13 chr4: 75,050,887-75,050,887 MTHFD2L
    nsv5694312mobile element insertion1nstd211human GRCh38 chr4: 74,144,878-74,144,878 , GRCh37.p13 chr4: 75,010,595-75,010,595 MTHFD2L
    nsv5693933mobile element insertion2nstd211human GRCh38 chr4: 74,129,787-74,129,787 , GRCh37.p13 chr4: 74,995,504-74,995,504 LOC105377277, MTHFD2L
    nsv5689109mobile element insertion2nstd211human GRCh38 chr4: 74,203,217-74,203,217 , GRCh37.p13 chr4: 75,068,934-75,068,934 MTHFD2L
    nsv5680694mobile element insertion1nstd211human GRCh38 chr4: 74,139,807-74,139,807 , GRCh37.p13 chr4: 75,005,524-75,005,524 MTHFD2L
    nsv5680570mobile element insertion1nstd211human GRCh38 chr4: 74,174,005-74,174,005 , GRCh37.p13 chr4: 75,039,722-75,039,722 MTHFD2L
    nsv5677384mobile element insertion1nstd211human GRCh38 chr4: 74,155,802-74,155,802 , GRCh37.p13 chr4: 75,021,519-75,021,519 MTHFD2L
    nsv5677366mobile element insertion1nstd211human GRCh38 chr4: 74,194,041-74,194,041 , GRCh37.p13 chr4: 75,059,758-75,059,758 MTHFD2L
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5622783insertion1nstd207human GRCh38 chr4: 74,203,200-74,203,200 , GRCh37.p13 chr4: 75,068,917-75,068,917 MTHFD2L
    nsv5622352insertion2nstd207human GRCh38 chr4: 74,188,742-74,188,742 , GRCh37.p13 chr4: 75,054,459-75,054,459 MTHFD2L
    nsv5621887insertion1nstd207human GRCh38 chr4: 74,217,808-74,217,808 , GRCh37.p13 chr4: 75,083,525-75,083,525 MTHFD2L
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