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Items: 1 to 20 of 272

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7144384insertion1nstd232human GRCh37.p13 chr3: 107,881,502-107,881,502 , GRCh38.p12 chr3: 108,162,655-108,162,655 IFT57
    nsv7139932insertion1nstd232human GRCh37.p13 chr3: 107,881,503-107,881,503 , GRCh38.p12 chr3: 108,162,656-108,162,656 IFT57
    nsv7047003inversion1nstd229human GRCh38 chr3: 105,966,506-108,938,496 , GRCh37.p13 chr3: 105,685,353-108,657,343 MTND4P16, CD47, 41 more genes
    nsv7042841inversion1nstd229human GRCh38 chr3: 104,903,601-112,515,639 , GRCh37.p13 chr3: 104,622,445-112,234,486 MTND4P16, CD47, 94 more genes
    nsv6717363copy number variation1nstd229human GRCh38 chr3: 108,157,468-108,164,717 , GRCh37.p13 chr3: 107,876,315-107,883,564 IFT57
    nsv6710492copy number variation1nstd229human GRCh38 chr3: 108,168,175-108,182,716 , GRCh37.p13 chr3: 107,887,022-107,901,563 IFT57
    nsv6709378copy number variation1nstd229human GRCh38 chr3: 107,392,201-108,950,478 , GRCh37.p13 chr3: 107,111,048-108,669,325 RPL13P8, RETNLB, 17 more genes
    nsv6707909copy number variation1nstd229human GRCh38 chr3: 108,179,150-108,496,000 , GRCh37.p13 chr3: 107,897,997-108,214,847 IFT57, HHLA2, 2 more genes
    nsv6705036copy number variation1nstd229human GRCh38 chr3: 108,167,145-108,172,158 , GRCh37.p13 chr3: 107,885,992-107,891,005 IFT57
    nsv6704750copy number variation1nstd229human GRCh38 chr3: 108,195,215-108,197,822 , GRCh37.p13 chr3: 107,914,062-107,916,669 IFT57
    nsv6702293copy number variation1nstd229human GRCh38 chr3: 108,183,900-108,184,229 , GRCh37.p13 chr3: 107,902,747-107,903,076 IFT57
    nsv6699632copy number variation1nstd229human GRCh38 chr3: 108,066,673-108,685,956 , GRCh37.p13 chr3: 107,785,520-108,404,803 LOC105374031, RPL13P8, 8 more genes
    nsv6698338copy number variation1nstd229human GRCh38 chr3: 108,068,211-108,497,947 , GRCh37.p13 chr3: 107,787,058-108,216,794 LOC105374031, HNRNPA1P17, 5 more genes
    nsv6636830copy number variation1nstd102humanPathogenic GRCh37 chr3: 107,059,705-115,005,256 , GRCh38.p12 chr3: 107,340,858-115,286,409 ATP6V1A, DRD3, 117 more genes
    nsv6628254copy number variation1nstd224human GRCh37 chr3: 106,647,916-112,127,787 , GRCh38.p12 chr3: 106,929,069-112,408,940 CD47, CD96, 71 more genes
    nsv6374011copy number variation1nstd223human GRCh38 chr3: 108,182,288-108,182,601 , GRCh37.p13 chr3: 107,901,135-107,901,448 IFT57
    nsv6370983copy number variation1nstd223human GRCh38 chr3: 108,179,563-108,180,225 , GRCh37.p13 chr3: 107,898,410-107,899,072 IFT57
    nsv6367385copy number variation1nstd223human GRCh38 chr3: 108,160,077-108,160,826 , GRCh37.p13 chr3: 107,878,924-107,879,673 IFT57
    nsv6357154copy number variation1nstd223human GRCh38 chr3: 108,167,145-108,172,156 , GRCh37.p13 chr3: 107,885,992-107,891,003 IFT57
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