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Items: 1 to 20 of 216

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923971copy number variation1nstd209human GRCh38 chr9: 113,090,630-113,127,171 , GRCh37.p13 chr9: 115,852,910-115,889,451 FAM225B, FAM225A
    nsv5867101copy number variation2nstd209human GRCh38 chr9: 113,090,962-113,105,251 , GRCh37.p13 chr9: 115,853,242-115,867,531 FAM225B
    nsv5851379copy number variation1nstd209human GRCh38 chr9: 113,102,599-113,132,758 , GRCh37.p13 chr9: 115,864,879-115,895,038 FAM225A, FAM225B
    nsv5848598copy number variation2nstd209human GRCh38 chr9: 113,096,262-113,103,023 , GRCh37.p13 chr9: 115,858,542-115,865,303 FAM225B
    nsv5670983inversion1nstd207human GRCh38 chr9: 113,105,213-113,119,362 , GRCh37.p13 chr9: 115,867,493-115,881,642 FAM225A, FAM225B
    nsv5555683inversion1nstd206human GRCh38 chr9: 113,104,987-113,119,565 , GRCh37.p13 chr9: 115,867,267-115,881,845 FAM225A, FAM225B
    nsv5492972copy number variation1nstd206human GRCh38 chr9: 113,111,542-113,112,045 , GRCh37.p13 chr9: 115,873,822-115,874,325 FAM225B, FAM225A
    nsv5487714copy number variation1nstd206human GRCh38 chr9: 113,089,900-113,122,600 , GRCh37.p13 chr9: 115,852,180-115,884,880 FAM225B, FAM225A
    nsv5484891copy number variation1nstd206human GRCh38 chr9: 113,096,552-113,107,000 , GRCh37.p13 chr9: 115,858,832-115,869,280 FAM225B
    nsv5483005copy number variation1nstd206human GRCh38 chr9: 113,090,787-113,127,173 , GRCh37.p13 chr9: 115,853,067-115,889,453 FAM225B, FAM225A
    nsv5475558copy number variation1nstd206human GRCh38 chr9: 113,089,663-113,107,052 , GRCh37.p13 chr9: 115,851,943-115,869,332 FAM225B
    nsv5379481translocation1nstd200human GRCh38 chr9: 113,111,683-113,111,683 , GRCh38 chr9: 113,119,466-113,119,466 , GRCh37.p13 chr9: 115,881,746-115,881,746 , GRCh37.p13 chr9: 115,873,963-115,873,963 FAM225A, FAM225B
    nsv5379480translocation1nstd200human GRCh38 chr9: 113,103,224-113,103,224 , GRCh38 chr9: 113,123,976-113,123,976 , GRCh37.p13 chr9: 115,886,256-115,886,256 , GRCh37.p13 chr9: 115,865,504-115,865,504 FAM225B
    nsv5343363translocation1nstd200human GRCh37 chr9: 115,881,746-115,881,746 , GRCh37 chr9: 115,873,963-115,873,963 , GRCh38.p12 chr9: 113,111,683-113,111,683 , GRCh38.p12 chr9: 113,119,466-113,119,466 FAM225B, FAM225A
    nsv5258926copy number variation1nstd204human GRCh38.p13 chr9: 113,089,643-113,119,332 , GRCh37.p13 chr9: 115,851,923-115,881,612 FAM225A, FAM225B
    nsv5255679copy number variation1nstd204human GRCh38.p13 chr9: 113,103,474-113,137,531 , GRCh37.p13 chr9: 115,865,754-115,899,811 FAM225B, FAM225A
    nsv5254384copy number variation1nstd204human GRCh38.p13 chr9: 113,111,701-113,113,200 , GRCh37.p13 chr9: 115,873,981-115,875,480 FAM225B, FAM225A
    nsv5244210copy number variation1nstd204human GRCh38.p13 chr9: 113,109,801-113,114,100 , GRCh37.p13 chr9: 115,872,081-115,876,380 FAM225A, FAM225B
    nsv5244026copy number variation1nstd204human GRCh38.p13 chr9: 113,090,201-113,106,200 , GRCh37.p13 chr9: 115,852,481-115,868,480 FAM225B
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
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