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Items: 1 to 20 of 275

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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
    nsv7056801inversion1nstd229human GRCh38 chr3: 108,317,549-108,318,270 , GRCh37.p13 chr3: 108,036,396-108,037,117 HHLA2
    nsv7047003inversion1nstd229human GRCh38 chr3: 105,966,506-108,938,496 , GRCh37.p13 chr3: 105,685,353-108,657,343 MTND4P16, CD47, 41 more genes
    nsv7046343inversion1nstd229human GRCh38 chr3: 108,261,187-113,011,016 , GRCh37.p13 chr3: 107,980,034-112,729,863 LOC105374041, DIMT1P1, 69 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
    nsv7042363inversion1nstd229human GRCh38 chr3: 108,304,729-108,307,428 , GRCh37.p13 chr3: 108,023,576-108,026,275 HHLA2
    nsv6717003copy number variation1nstd229human GRCh38 chr3: 108,303,526-108,306,261 , GRCh37.p13 chr3: 108,022,373-108,025,108 HHLA2
    nsv6716779copy number variation1nstd229human GRCh38 chr3: 108,266,365-108,735,273 , GRCh37.p13 chr3: 107,985,212-108,454,120 HNRNPA1P17, HHLA2, 5 more genes
    nsv6715941copy number variation1nstd229human GRCh38 chr3: 108,363,901-108,365,700 , GRCh37.p13 chr3: 108,082,748-108,084,547 HHLA2
    nsv6714145copy number variation1nstd229human GRCh38 chr3: 108,352,881-108,473,844 , GRCh37.p13 chr3: 108,071,728-108,192,691 MYH15, HHLA2
    nsv6711783copy number variation1nstd229human GRCh38 chr3: 108,317,534-108,464,628 , GRCh37.p13 chr3: 108,036,381-108,183,475 HNRNPA1P17, MYH15, 1 more genes
    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
    nsv6707521copy number variation1nstd229human GRCh38 chr3: 108,295,529-108,336,411 , GRCh37.p13 chr3: 108,014,376-108,055,258 HNRNPA1P17, HHLA2
    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
    nsv6699569copy number variation1nstd229human GRCh38 chr3: 108,318,424-108,323,624 , GRCh37.p13 chr3: 108,037,271-108,042,471 HNRNPA1P17, HHLA2
    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
    nsv6575353inversion1nstd223human GRCh38 chr3: 108,317,635-108,318,193 , GRCh37.p13 chr3: 108,036,482-108,037,040 HHLA2
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