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Items: 1 to 20 of 252

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093619copy number variation1nstd228human GRCh37 chr4: 171,508,974-190,957,473 , GRCh38.p12 chr4: 170,587,823-190,036,318 AGA, SLC25A4, 240 more genes
    nsv7056086inversion1nstd229human GRCh38 chr4: 174,912,619-184,252,538 , GRCh37.p13 chr4: 175,833,770-185,173,691 WDR17, LOC105377580, 84 more genes
    nsv7055054inversion1nstd229human GRCh38 chr4: 177,546,174-183,679,474 , GRCh37.p13 chr4: 178,467,328-184,600,627 RNU6-479P, VTI1BP2, 52 more genes
    nsv7054725inversion1nstd229human GRCh38 chr4: 178,850,585-188,333,056 , GRCh37.p13 chr4: 179,771,739-189,254,210 RPL6P16, LOC105377568, 125 more genes
    nsv7052036inversion1nstd229human GRCh38 chr4: 180,230,319-182,805,344 , GRCh37.p13 chr4: 181,151,472-183,726,497 LOC105377572, LOC107986205, 16 more genes
    nsv7050592inversion1nstd229human GRCh38 chr4: 181,219,378-183,892,493 , GRCh37.p13 chr4: 182,140,531-184,813,646 ING2, VTI1BP2, 40 more genes
    nsv7048281inversion1nstd229human GRCh38 chr4: 177,590,230-186,282,308 , GRCh37.p13 chr4: 178,511,384-187,203,462 STOX2, LINC01098, 105 more genes
    nsv7041870inversion1nstd229human GRCh38 chr4: 182,134,437-182,137,042 , GRCh37.p13 chr4: 183,055,590-183,058,195 TENM3, TENM3-AS1
    nsv6754796copy number variation1nstd229human GRCh38 chr4: 180,175,444-182,173,043 , GRCh37.p13 chr4: 181,096,597-183,094,196 MIR1305, TENM3-AS2, 12 more genes
    nsv6748250copy number variation1nstd229human GRCh38 chr4: 179,729,233-182,727,604 , GRCh37.p13 chr4: 180,650,386-183,648,757 RNU2-34P, LOC105377567, 15 more genes
    nsv6743919copy number variation1nstd229human GRCh38 chr4: 180,245,568-182,136,896 , GRCh37.p13 chr4: 181,166,721-183,058,049 LOC132386, NDUFB5P1, 11 more genes
    nsv6634364copy number variation1nstd102humanPathogenic GRCh37 chr4: 167,779,888-190,957,473 , GRCh38.p12 chr4: 166,858,737-190,036,318 LOC101928551, LOC107986330, 279 more genes
    nsv6634351copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318 COPS3P1, LOC339975, 363 more genes
    nsv6382005copy number variation1nstd223human GRCh38 chr4: 179,729,231-182,727,604 , GRCh37.p13 chr4: 180,650,384-183,648,757 LOC132386, CCNHP1, 15 more genes
    nsv6315348copy number variation1nstd102humanPathogenic GRCh37 chr4: 174,944,132-190,957,473 , GRCh38.p12 chr4: 174,022,981-190,036,318 SPATA4, ADAM20P2, 203 more genes
    nsv6314781copy number variation1nstd220human GRCh38.p12 chr4: 181,774,580-188,158,025 , GRCh37 chr4: 182,695,733-189,079,179 , SLC25A4, 117 more genes
    nsv6313766copy number variation1nstd102humanUncertain significance GRCh37 chr4: 182,811,256-184,082,842 , GRCh38.p12 chr4: 181,890,103-183,161,689 MIR1305, TENM3-AS1, 17 more genes
    nsv6313729copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,755,174-190,225,765 , GRCh38.p12 chr4: 158,834,022-189,304,611 NAF1, LOC107986200, 336 more genes
    nsv6313663copy number variation1nstd102humanPathogenic GRCh37 chr4: 175,855,408-190,957,473 , GRCh38.p12 chr4: 174,934,257-190,036,318 LINC01596, NDUFB5P1, 190 more genes
    nsv6291245copy number variation1nstd102humanUncertain significance GRCh37 chr4: 180,650,411-183,647,536 , GRCh38.p12 chr4: 179,729,258-182,726,383 LOC105377572, LOC107986205, 15 more genes
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