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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057933inversion1nstd229human GRCh38 chr7: 63,377,139-65,038,693 , GRCh37.p13 chr7: 62,837,517-64,499,071 , VN1R36P, 91 more genes
    nsv7044033inversion1nstd229human GRCh38 chr7: 64,403,303-64,515,371 , GRCh37.p13 chr7: 63,863,681-63,975,749 HNRNPCP7, VN1R40P, 5 more genes
    nsv6836335copy number variation1nstd229human GRCh38 chr7: 64,461,872-64,498,772 , GRCh37.p13 chr7: 63,922,250-63,959,150 VN1R41P, ZNF680P1, 1 more genes
    nsv6831745copy number variation1nstd229human GRCh38 chr7: 64,469,316-64,494,523 , GRCh37.p13 chr7: 63,929,694-63,954,901 VN1R41P, ZNF680P1
    nsv6830203copy number variation1nstd229human GRCh38 chr7: 64,218,996-64,547,325 , GRCh37.p13 chr7: 63,679,374-64,007,703 LOC105375321, LOC105375324, 14 more genes
    nsv6827445copy number variation1nstd229human GRCh38 chr7: 64,410,501-64,515,400 , GRCh37.p13 chr7: 63,870,879-63,975,778 YWHAEP1, HNRNPCP7, 5 more genes
    nsv6818340copy number variation1nstd229human GRCh38 chr7: 64,462,374-64,808,082 , GRCh37.p13 chr7: 63,922,752-64,268,460 LOC100133092, ZNF138, 13 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6632418copy number variation3nstd224human GRCh37 chr7: 63,758,482-63,962,963 , GRCh38.p12 chr7: 64,298,104-64,502,585 ZNF680, ZNF736, 9 more genes
    nsv6632417copy number variation1nstd224human GRCh37 chr7: 63,352,782-63,962,963 , GRCh38.p12 chr7: 63,892,404-64,502,585 RPL6P20, ZNF680, 43 more genes
    nsv6632413copy number variation1nstd224human GRCh37 chr7: 62,241,041-64,438,809 , GRCh38.p12 chr7: 62,780,663-64,978,431 , ZNF138, 99 more genes
    nsv6611133copy number variation1nstd223human GRCh38 chr7: 64,461,872-64,498,769 , GRCh37.p13 chr7: 63,922,250-63,959,147 VN1R41P, ZNF680, 1 more genes
    nsv6608734copy number variation1nstd223human GRCh38 chr7: 64,468,176-64,470,738 , GRCh37.p13 chr7: 63,928,554-63,931,116 ZNF680P1
    nsv6606011copy number variation1nstd223human GRCh38 chr7: 64,466,947-64,468,219 , GRCh37.p13 chr7: 63,927,325-63,928,597 ZNF680P1
    nsv6570029inversion1nstd223human GRCh38 chr7: 64,466,999-64,468,407 , GRCh37.p13 chr7: 63,927,377-63,928,785 ZNF680P1
    nsv6564244inversion1nstd223human GRCh38 chr7: 64,468,327-64,468,826 , GRCh37.p13 chr7: 63,928,705-63,929,204 ZNF680P1
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6303490copy number variation1nstd186human GRCh37 chr7: 63,924,938-63,935,636 , GRCh38.p12 chr7: 64,464,560-64,475,258 VN1R41P, ZNF680P1
    nsv6136259copy number variation1nstd213human GRCh37 chr7: 63,890,000-64,210,001 , GRCh38.p12 chr7: 64,429,622-64,749,623 LOC641746, LOC644387, 14 more genes
    nsv6136196copy number variation1nstd213human GRCh37 chr7: 62,900,000-64,980,001 , GRCh38.p12 chr7: 63,439,622-65,515,088 , ZNF138, 95 more genes
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