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Items: 1 to 20 of 259

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7051507inversion1nstd229human GRCh38 chr5: 44,302,285-44,306,528 , GRCh37.p13 chr5: 44,302,387-44,306,630 FGF10
    nsv7040713inversion1nstd229human GRCh38 chr5: 44,325,839-45,047,347 , GRCh37.p13 chr5: 44,325,941-45,047,449 MRPS30, FGF10, 4 more genes
    nsv6774462copy number variation1nstd229human GRCh38 chr5: 44,344,280-44,344,921 , GRCh37.p13 chr5: 44,344,382-44,345,023 FGF10
    nsv6772412copy number variation1nstd229human GRCh38 chr5: 44,342,530-44,348,603 , GRCh37.p13 chr5: 44,342,632-44,348,705 FGF10
    nsv6769384copy number variation1nstd229human GRCh38 chr5: 44,302,423-44,304,303 , GRCh37.p13 chr5: 44,302,525-44,304,405 FGF10
    nsv6767742copy number variation1nstd229human GRCh38 chr5: 44,362,501-44,370,800 , GRCh37.p13 chr5: 44,362,603-44,370,902 FGF10
    nsv6767697copy number variation1nstd229human GRCh38 chr5: 44,333,482-44,333,670 , GRCh37.p13 chr5: 44,333,584-44,333,772 FGF10
    nsv6764957copy number variation1nstd229human GRCh38 chr5: 44,285,715-44,316,547 , GRCh37.p13 chr5: 44,285,817-44,316,649 FGF10
    nsv6763415copy number variation1nstd229human GRCh38 chr5: 44,343,224-44,349,488 , GRCh37.p13 chr5: 44,343,326-44,349,590 FGF10
    nsv6636973copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,348,753-46,389,339 , GRCh38.p12 chr5: 29,348,646-46,389,237 SUB1, LOC105374740, 210 more genes
    nsv6395493copy number variation1nstd223human GRCh38 chr5: 44,342,533-44,348,601 , GRCh37.p13 chr5: 44,342,635-44,348,703 FGF10
    nsv6395225copy number variation1nstd223human GRCh38 chr5: 44,315,424-44,315,906 , GRCh37.p13 chr5: 44,315,526-44,316,008 FGF10
    nsv6394658copy number variation1nstd223human GRCh38 chr5: 44,344,278-44,344,920 , GRCh37.p13 chr5: 44,344,380-44,345,022 FGF10
    nsv6394113copy number variation1nstd223human GRCh38 chr5: 44,310,047-44,310,574 , GRCh37.p13 chr5: 44,310,149-44,310,676 FGF10
    nsv6392627copy number variation1nstd223human GRCh38 chr5: 44,333,053-44,333,679 , GRCh37.p13 chr5: 44,333,155-44,333,781 FGF10
    nsv6390621copy number variation1nstd223human GRCh38 chr5: 43,938,265-44,306,135 , GRCh37.p13 chr5: 43,938,367-44,306,237 RNU6-381P, FGF10
    nsv6384729copy number variation1nstd223human GRCh38 chr5: 44,340,008-44,340,321 , GRCh37.p13 chr5: 44,340,110-44,340,423 FGF10
    nsv6382665copy number variation1nstd223human GRCh38 chr5: 44,317,559-44,322,216 , GRCh37.p13 chr5: 44,317,661-44,322,318 FGF10
    nsv6379992copy number variation1nstd223human GRCh38 chr5: 44,334,801-44,336,500 , GRCh37.p13 chr5: 44,334,903-44,336,602 FGF10
    nsv6378920copy number variation1nstd223human GRCh38 chr5: 44,380,973-44,381,445 , GRCh37.p13 chr5: 44,381,075-44,381,547 FGF10
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