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Items: 1 to 20 of 187

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7052737inversion1nstd229human GRCh38 chr4: 124,487,719-129,666,522 , GRCh37.p13 chr4: 125,408,874-130,587,677 H3P15, ANKRD50, 36 more genes
    nsv7043630inversion1nstd229human GRCh38 chr4: 127,283,753-130,065,798 , GRCh37.p13 chr4: 128,204,908-130,986,953 SCLT1, JADE1, 30 more genes
    nsv6752093copy number variation1nstd229human GRCh38 chr4: 128,283,033-128,286,465 , GRCh37.p13 chr4: 129,204,188-129,207,620 PGRMC2
    nsv6749539copy number variation1nstd229human GRCh38 chr4: 128,283,113-128,283,537 , GRCh37.p13 chr4: 129,204,268-129,204,692 PGRMC2
    nsv6749490copy number variation1nstd229human GRCh38 chr4: 128,287,331-128,445,058 , GRCh37.p13 chr4: 129,208,486-129,366,213 PGRMC2, LINC02615
    nsv6382691copy number variation1nstd223human GRCh38 chr4: 128,283,501-128,291,600 , GRCh37.p13 chr4: 129,204,656-129,212,755 PGRMC2
    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
    nsv6313750copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,888,785-129,649,979 , GRCh38.p12 chr4: 115,967,629-128,728,824 LOC105377395, SEPTIN7P14, 152 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
    nsv6290265copy number variation1nstd102humanPathogenic GRCh37 chr4: 114,872,547-138,005,267 , GRCh38.p12 chr4: 113,951,391-137,084,113 LOC105379404, IL21-AS1, 218 more genes
    nsv6255316mobile element insertion1nstd215human GRCh38 chr4: 128,286,093-128,286,093 , GRCh37.p13 chr4: 129,207,248-129,207,248 PGRMC2
    nsv6255315mobile element insertion1nstd215human GRCh38 chr4: 128,280,269-128,280,269 , GRCh37.p13 chr4: 129,201,424-129,201,424 PGRMC2
    nsv6255314mobile element insertion1nstd215human GRCh38 chr4: 128,272,603-128,272,603 , GRCh37.p13 chr4: 129,193,758-129,193,758 PGRMC2
    nsv6134884copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,720,001 , GRCh38.p12 chr4: 108,308,844-160,798,849 , ANK2, 616 more genes
    nsv6134731copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,710,001 , GRCh38.p12 chr4: 108,308,844-160,788,849 , ANK2, 616 more genes
    nsv6077510insertion1nstd212human GRCh38 chr4: 128,286,080-128,286,080 , GRCh37.p13 chr4: 129,207,235-129,207,235 PGRMC2
    nsv5965398insertion1nstd209human GRCh38 chr4: 128,286,080-128,286,080 , GRCh37.p13 chr4: 129,207,235-129,207,235 PGRMC2
    nsv5716512mobile element insertion1nstd211human GRCh38 chr4: 128,271,061-128,271,061 , GRCh37.p13 chr4: 129,192,216-129,192,216 PGRMC2
    nsv5692655mobile element insertion2nstd211human GRCh38 chr4: 128,286,093-128,286,093 , GRCh37.p13 chr4: 129,207,248-129,207,248 PGRMC2
    nsv5681173mobile element insertion2nstd211human GRCh38 chr4: 128,280,269-128,280,269 , GRCh37.p13 chr4: 129,201,424-129,201,424 PGRMC2
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