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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7045068inversion1nstd229human GRCh38 chr4: 138,588,072-141,319,129 , GRCh37.p13 chr4: 139,509,226-142,240,283 RN7SKP253, FTH1P24, 41 more genes
    nsv7043921inversion1nstd229human GRCh38 chr4: 140,360,921-141,000,145 , GRCh37.p13 chr4: 141,282,075-141,921,299 UCP1, CLGN, 10 more genes
    nsv7040945inversion1nstd229human GRCh38 chr4: 140,412,026-140,412,036 , GRCh37.p13 chr4: 141,333,180-141,333,190 CLGN
    nsv6749380copy number variation1nstd229human GRCh38 chr4: 140,009,175-140,578,062 , GRCh37.p13 chr4: 140,930,329-141,499,216 SCOC-AS1, ELMOD2, 8 more genes
    nsv6743912copy number variation1nstd229human GRCh38 chr4: 140,226,102-140,524,180 , GRCh37.p13 chr4: 141,147,256-141,445,334 ELMOD2, CLGN, 4 more genes
    nsv6571624inversion1nstd223human GRCh38 chr4: 140,362,302-141,000,082 , GRCh37.p13 chr4: 141,283,456-141,921,236 RN7SL152P, UCP1, 10 more genes
    nsv6569147inversion1nstd223human GRCh38 chr4: 140,397,902-140,398,270 , GRCh37.p13 chr4: 141,319,056-141,319,424 CLGN
    nsv6562176inversion1nstd223human GRCh38 chr4: 140,394,873-140,395,241 , GRCh37.p13 chr4: 141,316,027-141,316,395 CLGN
    nsv6559786inversion1nstd223human GRCh38 chr4: 140,360,921-141,000,145 , GRCh37.p13 chr4: 141,282,075-141,921,299 TNRC18P1, RNY1P14, 10 more genes
    nsv6390838copy number variation1nstd223human GRCh38 chr4: 140,401,301-140,403,400 , GRCh37.p13 chr4: 141,322,455-141,324,554 CLGN
    nsv6383734copy number variation1nstd223human GRCh38 chr4: 140,415,201-140,437,200 , GRCh37.p13 chr4: 141,336,355-141,358,354 CLGN
    nsv6378471copy number variation1nstd223human GRCh38 chr4: 140,215,978-145,835,229 , GRCh37.p13 chr4: 141,137,132-146,756,381 OTUD4, GYPA, 62 more genes
    nsv6313878copy number variation1nstd102humanPathogenic GRCh37 chr4: 104,715,235-145,252,595 , GRCh38.p12 chr4: 103,794,078-144,331,443 LINC00613, GYPA, 448 more genes
    nsv6313656copy number variation1nstd102humanUncertain significance GRCh37 chr4: 136,035,308-144,718,930 , GRCh38.p12 chr4: 135,114,153-143,797,777 RPS2P20, LOC105377444, 87 more genes
    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
    nsv6291168copy number variation1nstd102humanPathogenic GRCh37 chr4: 138,289,049-145,923,298 , GRCh38.p12 chr4: 137,367,895-145,002,146 LOC105377447, RN7SKP253, 92 more genes
    nsv6290718copy number variation1nstd102humanPathogenic GRCh37 chr4: 136,529,470-141,564,812 , GRCh38.p12 chr4: 135,608,315-140,643,658 MGARP, NAA15, 61 more genes
    nsv6255420mobile element insertion1nstd215human GRCh38 chr4: 140,401,699-140,401,699 , GRCh37.p13 chr4: 141,322,853-141,322,853 CLGN
    nsv6135293copy number variation1nstd213human GRCh37 chr4: 141,260,000-141,610,001 , GRCh38.p12 chr4: 140,338,846-140,688,847 CLGN, UCP1, 8 more genes
    nsv6134910copy number variation1nstd213human GRCh37 chr4: 140,660,000-141,870,001 , GRCh38.p12 chr4: 139,738,846-140,948,847 CLGN, MGST2, 15 more genes
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