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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5911740copy number variation1nstd209human GRCh38 chr10: 13,345,026-13,347,996 , GRCh37.p13 chr10: 13,387,026-13,389,996 SEPHS1
    nsv5701375mobile element insertion1nstd211human GRCh38 chr10: 13,316,701-13,316,701 , GRCh37.p13 chr10: 13,358,701-13,358,701 SEPHS1
    nsv5700155mobile element insertion1nstd211human GRCh38 chr10: 13,326,961-13,326,961 , GRCh37.p13 chr10: 13,368,961-13,368,961 SEPHS1
    nsv5553139insertion1nstd206human GRCh38 chr10: 13,326,961-13,327,001 , GRCh37.p13 chr10: 13,368,961-13,369,001 SEPHS1
    nsv5402815mobile element insertion1nstd206human GRCh38 chr10: 13,316,701-13,316,752 , GRCh37.p13 chr10: 13,358,701-13,358,752 SEPHS1
    nsv5381768copy number variation1nstd102humanPathogenic GRCh37 chr10: 9,137,489-17,227,168 , GRCh38.p12 chr10: 9,095,526-17,185,169 PROSER2, C1QL3, 110 more genes
    nsv5372383translocation1nstd200human GRCh38 chr9: 27,027,509-27,027,509 , GRCh38 chr10: 13,317,438-13,317,438 , GRCh37.p13 chr10: 13,359,438-13,359,438 , GRCh37.p13 chr9: 27,027,507-27,027,507 IFT74, SEPHS1
    nsv5364765translocation1nstd200human GRCh38 chr10: 13,318,965-13,318,965 , GRCh38 chr14: 51,553,069-51,553,069 , GRCh37.p13 chr10: 13,360,965-13,360,965 , GRCh37.p13 chr14: 52,019,787-52,019,787 SEPHS1, FRMD6, 1 more genes
    nsv5364764translocation1nstd200human GRCh38 chr13: 36,332,763-36,332,763 , GRCh38 chr10: 13,318,080-13,318,080 , GRCh37.p13 chr10: 13,360,080-13,360,080 , GRCh37.p13 chr13: 36,906,900-36,906,900 SEPHS1, SPART
    nsv5347432translocation1nstd200human GRCh38 chr9: 27,027,498-27,027,498 , GRCh38 chr10: 13,348,213-13,348,213 , GRCh37.p13 chr10: 13,390,213-13,390,213 , GRCh37.p13 chr9: 27,027,496-27,027,496 SEPHS1, IFT74
    nsv5345790translocation1nstd200human GRCh37 chr10: 13,359,438-13,359,438 , GRCh37 chr9: 27,027,507-27,027,507 , GRCh38.p12 chr9: 27,027,509-27,027,509 , GRCh38.p12 chr10: 13,317,438-13,317,438 SEPHS1, IFT74
    nsv5333774translocation1nstd200human GRCh37 chr10: 13,390,213-13,390,213 , GRCh37 chr9: 27,027,496-27,027,496 , GRCh38.p12 chr10: 13,348,213-13,348,213 , GRCh38.p12 chr9: 27,027,498-27,027,498 SEPHS1, IFT74
    nsv5139221mobile element insertion1nstd203human GRCh38 chr10: 13,325,909-13,325,928 , GRCh37.p13 chr10: 13,367,909-13,367,928 SEPHS1
    nsv5124296mobile element insertion1nstd203human GRCh38 chr10: 13,325,894-13,325,933 , GRCh37.p13 chr10: 13,367,894-13,367,933 SEPHS1
    nsv5121216mobile element insertion1nstd203human GRCh38 chr10: 13,325,895-13,325,933 , GRCh37.p13 chr10: 13,367,895-13,367,933 SEPHS1
    nsv4975014copy number variation1nstd200human GRCh38 chr10: 13,347,230-13,347,330 , GRCh37.p13 chr10: 13,389,230-13,389,330 SEPHS1
    nsv4683475copy number variation1nstd102humanUncertain significance GRCh37 chr10: 13,320,301-13,371,788 , GRCh38.p12 chr10: 13,278,301-13,329,788 PHYH, RBISP1, 1 more genes
    nsv4538554insertion1nstd166human GRCh37.p13 chr10: 13,358,684-13,358,684 , GRCh38.p12 chr10: 13,316,684-13,316,684 SEPHS1
    nsv4455607copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,026-15,273,144 , GRCh38.p12 chr10: 54,086-15,231,145 LOC105376357, LINC02649, 264 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
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