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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5688682mobile element insertion1nstd211human GRCh38 chr4: 52,037,868-52,037,868 , GRCh37.p13 chr4: 52,904,034-52,904,034 SGCB
    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
    nsv5409621mobile element insertion1nstd206human GRCh38 chr4: 52,037,868-52,037,919 , GRCh37.p13 chr4: 52,904,034-52,904,085 SGCB
    nsv5098991mobile element insertion1nstd203human GRCh38 chr4: 52,034,327-52,034,347 , GRCh37.p13 chr4: 52,900,493-52,900,513 SGCB
    nsv5091961mobile element insertion1nstd203human GRCh38 chr4: 52,034,348-52,034,370 , GRCh37.p13 chr4: 52,900,514-52,900,536 SGCB
    nsv5086099mobile element insertion1nstd203human GRCh38 chr4: 52,019,849-52,019,864 , GRCh37.p13 chr4: 52,886,015-52,886,030 SGCB, LRRC66
    nsv5083534mobile element insertion1nstd203human GRCh38 chr4: 52,034,350-52,034,368 , GRCh37.p13 chr4: 52,900,516-52,900,534 SGCB
    nsv5080085mobile element insertion1nstd203human GRCh38 chr4: 52,034,331-52,034,366 , GRCh37.p13 chr4: 52,900,497-52,900,532 SGCB
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4913258copy number variation1nstd200human GRCh38 chr4: 52,025,785-52,025,909 , GRCh37.p13 chr4: 52,891,951-52,892,075 SGCB
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4791614copy number variation1nstd200human GRCh37 chr4: 43,358,175-53,119,711 , GRCh38.p12 chr4: 43,356,158-52,253,545 , LOC107986277, 78 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4682626copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr4: 52,899,587-52,899,816 , GRCh38.p12 chr4: 52,033,421-52,033,650 SGCB
    nsv4591207copy number variation1nstd183human GRCh37 chr4: 52,685,699-53,586,480 , GRCh38.p12 chr4: 51,819,533-52,720,313 , SNORA26, 14 more genes
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