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Items: 1 to 20 of 198

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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
    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
    nsv6559786inversion1nstd223human GRCh38 chr4: 140,360,921-141,000,145 , GRCh37.p13 chr4: 141,282,075-141,921,299 TNRC18P1, RNY1P14, 10 more genes
    nsv6395064copy number variation1nstd223human GRCh38 chr4: 140,550,804-140,551,317 , GRCh37.p13 chr4: 141,471,958-141,472,471 ELMOD2
    nsv6388841copy number variation1nstd223human GRCh38 chr4: 140,518,401-140,529,300 , GRCh37.p13 chr4: 141,439,555-141,450,454 ELMOD2
    nsv6388570copy number variation1nstd223human GRCh38 chr4: 140,548,536-140,548,955 , GRCh37.p13 chr4: 141,469,690-141,470,109 ELMOD2
    nsv6385114copy number variation1nstd223human GRCh38 chr4: 140,540,438-140,541,093 , GRCh37.p13 chr4: 141,461,592-141,462,247 ELMOD2
    nsv6384244copy number variation1nstd223human GRCh38 chr4: 140,530,101-140,531,200 , GRCh37.p13 chr4: 141,451,255-141,452,354 ELMOD2
    nsv6382421copy number variation1nstd223human GRCh38 chr4: 140,550,101-140,552,800 , GRCh37.p13 chr4: 141,471,255-141,473,954 ELMOD2
    nsv6381447copy number variation1nstd223human GRCh38 chr4: 140,542,253-140,542,740 , GRCh37.p13 chr4: 141,463,407-141,463,894 ELMOD2
    nsv6379033copy number variation1nstd223human GRCh38 chr4: 140,551,001-140,552,600 , GRCh37.p13 chr4: 141,472,155-141,473,754 ELMOD2
    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
    nsv6377662copy number variation1nstd223human GRCh38 chr4: 140,551,469-140,552,148 , GRCh37.p13 chr4: 141,472,623-141,473,302 ELMOD2
    nsv6376542copy number variation1nstd223human GRCh38 chr4: 140,492,201-140,537,400 , GRCh37.p13 chr4: 141,413,355-141,458,554 ELMOD2, MGAT4D
    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
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