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Items: 1 to 20 of 249

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7097256copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr4: 55,124,936-57,368,027 , GRCh38.p12 chr4: 54,258,769-56,501,861 AASDH, EXOC1, 40 more genes
    nsv7042838inversion1nstd229human GRCh38 chr4: 55,519,343-61,509,140 , GRCh37.p13 chr4: 56,385,510-62,374,858 LINC02271, CHAER1, 59 more genes
    nsv6737599copy number variation1nstd229human GRCh38 chr4: 55,595,305-55,609,280 , GRCh37.p13 chr4: 56,461,472-56,475,447 NMU
    nsv6727111copy number variation1nstd229human GRCh38 chr4: 55,600,801-55,645,200 , GRCh37.p13 chr4: 56,466,968-56,511,367 NMU
    nsv6725591copy number variation1nstd229human GRCh38 chr4: 55,515,301-55,598,400 , GRCh37.p13 chr4: 56,381,468-56,464,567 CLOCK, RN7SKP30, 2 more genes
    nsv6723357copy number variation1nstd229human GRCh38 chr4: 55,591,407-55,595,750 , GRCh37.p13 chr4: 56,457,574-56,461,917 NMU, PDCL2
    nsv6722401copy number variation1nstd229human GRCh38 chr4: 55,556,580-55,828,542 , GRCh37.p13 chr4: 56,422,747-56,694,708 EXOC1L, LOC105377661, 4 more genes
    nsv6720279copy number variation1nstd229human GRCh38 chr4: 55,564,862-55,964,774 , GRCh37.p13 chr4: 56,431,029-56,830,940 EXOC1, NMU, 8 more genes
    nsv6637063copy number variation1nstd102humanUncertain significance GRCh37 chr4: 52,685,980-59,272,025 , GRCh38.p12 chr4: 51,819,814-58,405,859 SPINK2, RN7SL492P, 100 more genes
    nsv6629496copy number variation1nstd224human GRCh37 chr4: 56,471,433-56,482,507 , GRCh38.p12 chr4: 55,605,266-55,616,340 NMU
    nsv6395526copy number variation1nstd223human GRCh38 chr4: 55,591,407-55,595,745 , GRCh37.p13 chr4: 56,457,574-56,461,912 PDCL2, NMU
    nsv6384749copy number variation1nstd223human GRCh38 chr4: 55,600,101-55,601,600 , GRCh37.p13 chr4: 56,466,268-56,467,767 NMU
    nsv6384233copy number variation1nstd223human GRCh38 chr4: 55,603,008-55,604,233 , GRCh37.p13 chr4: 56,469,175-56,470,400 NMU
    nsv6315421copy number variation1nstd102humanPathogenic GRCh37 chr4: 53,688,710-56,491,447 , GRCh38.p12 chr4: 52,822,543-55,625,280 METTL5P3, RPL38P3, 38 more genes
    nsv6311837copy number variation2nstd102humanUncertain significance GRCh37 chr4: 55,124,936-57,798,318 , GRCh38.p12 chr4: 54,258,769-56,932,152 GLDCP1, KDR, 54 more genes
    nsv6295601copy number variation1nstd186human GRCh37 chr4: 56,469,016-56,470,399 , GRCh38.p12 chr4: 55,602,849-55,604,232 NMU
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6291206copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,685,685-58,104,722 , GRCh38.p12 chr4: 51,819,519-57,238,556 SRD5A3, DCUN1D4, 96 more genes
    nsv6279776insertion2nstd214human GRCh38 chr4: 55,604,017-55,604,017 , GRCh37.p13 chr4: 56,470,184-56,470,184 NMU
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