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Items: 1 to 20 of 199

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7098893copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,610,933-135,439,810 , GRCh38.p12 chr10: 120,851,421-133,626,306 LOC105378571, DOCK1, 196 more genes
    nsv7093623copy number variation1nstd102humanUncertain significance GRCh37 chr10: 123,239,371-124,813,281 , GRCh38.p12 chr10: 121,479,857-123,053,765 TACC2, BTBD16, 25 more genes
    nsv7068192inversion1nstd229human GRCh38 chr10: 118,910,158-125,783,778 , GRCh37.p13 chr10: 120,669,670-127,472,347 CTBP2, RPS26P39, 114 more genes
    nsv6896038copy number variation1nstd229human GRCh38 chr10: 121,643,660-121,650,103 , GRCh37.p13 chr10: 123,403,174-123,409,617 LOC107984183
    nsv6895082copy number variation1nstd229human GRCh38 chr10: 121,637,435-121,644,770 , GRCh37.p13 chr10: 123,396,949-123,404,284 LOC107984183
    nsv6891810copy number variation1nstd229human GRCh38 chr10: 121,642,001-121,646,200 , GRCh37.p13 chr10: 123,401,515-123,405,714 LOC107984183
    nsv6891128copy number variation1nstd229human GRCh38 chr10: 121,644,001-121,650,100 , GRCh37.p13 chr10: 123,403,515-123,409,614 LOC107984183
    nsv6881313copy number variation1nstd229human GRCh38 chr10: 121,623,081-121,633,326 , GRCh37.p13 chr10: 123,382,595-123,392,840 LOC107984183
    nsv6880920copy number variation1nstd229human GRCh38 chr10: 121,643,501-121,651,200 , GRCh37.p13 chr10: 123,403,015-123,410,714 LOC107984183
    nsv6880797copy number variation1nstd229human GRCh38 chr10: 121,642,048-121,647,682 , GRCh37.p13 chr10: 123,401,562-123,407,196 LOC107984183
    nsv6879944copy number variation1nstd229human GRCh38 chr10: 121,503,205-121,896,746 , GRCh37.p13 chr10: 123,262,719-123,656,261 LOC107984183, ATE1, 2 more genes
    nsv6879242copy number variation1nstd229human GRCh38 chr10: 121,484,942-121,719,153 , GRCh37.p13 chr10: 123,244,456-123,478,667 FGFR2, RPS15AP5, 1 more genes
    nsv6593921inversion1nstd223human GRCh38 chr10: 121,642,311-121,643,471 , GRCh37.p13 chr10: 123,401,825-123,402,985 LOC107984183
    nsv6587556inversion1nstd223human GRCh38 chr10: 121,625,650-121,626,358 , GRCh37.p13 chr10: 123,385,164-123,385,872 LOC107984183
    nsv6585886inversion1nstd223human GRCh38 chr10: 118,910,158-125,783,778 , GRCh37.p13 chr10: 120,669,670-127,472,347 LOC105378520, SPADH, 114 more genes
    nsv6455468copy number variation1nstd223human GRCh38 chr10: 121,637,435-121,644,763 , GRCh37.p13 chr10: 123,396,949-123,404,277 LOC107984183
    nsv6444356copy number variation1nstd223human GRCh38 chr10: 121,619,443-121,621,996 , GRCh37.p13 chr10: 123,378,957-123,381,510 LOC107984183
    nsv6441473copy number variation1nstd223human GRCh38 chr10: 121,644,901-121,650,100 , GRCh37.p13 chr10: 123,404,415-123,409,614 LOC107984183
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