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Items: 1 to 20 of 115

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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
    nsv7093904copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,344,461-105,992,004 , GRCh38.p12 chr10: 97,584,704-104,232,246 ABCC2, LBX1-AS1, 160 more genes
    nsv7061391inversion1nstd229human GRCh38 chr10: 100,357,388-105,969,995 , GRCh37.p13 chr10: 102,117,145-107,729,753 , CALHM1, 127 more genes
    nsv6895230copy number variation1nstd229human GRCh38 chr10: 103,230,955-103,592,585 , GRCh37.p13 chr10: 104,990,712-105,352,342 RPEL1, CALHM3, 12 more genes
    nsv6891788copy number variation1nstd229human GRCh38 chr10: 103,205,994-103,520,342 , GRCh37.p13 chr10: 104,965,751-105,280,099 ATP5MK, PDCD11, 12 more genes
    nsv6883490copy number variation1nstd229human GRCh38 chr10: 103,473,024-103,475,638 , GRCh37.p13 chr10: 105,232,781-105,235,395 CALHM3
    nsv6880434copy number variation1nstd229human GRCh38 chr10: 103,302,516-106,977,869 , GRCh37.p13 chr10: 105,062,273-108,737,627 RNU11-3P, GSTO2, 48 more genes
    nsv6637523copy number variation1nstd102humanUncertain significance GRCh37 chr10: 105,015,345-105,911,204 , GRCh38.p12 chr10: 103,255,588-104,151,446 PCGF6, INA, 20 more genes
    nsv6620305copy number variation1nstd224human GRCh37 chr10: 105,154,089-105,294,641 , GRCh38.p12 chr10: 103,394,332-103,534,884 NEURL1, PDCD11, 6 more genes
    nsv6594978inversion1nstd223human GRCh38 chr10: 103,205,613-103,520,468 , GRCh37.p13 chr10: 104,965,370-105,280,225 ST13P13, CALHM1, 12 more genes
    nsv6446980copy number variation1nstd223human GRCh38 chr10: 103,473,262-103,482,173 , GRCh37.p13 chr10: 105,233,019-105,241,930 CALHM3, NEURL1-AS1
    nsv6440427copy number variation1nstd223human GRCh38 chr10: 103,392,774-103,551,394 , GRCh37.p13 chr10: 105,152,531-105,311,151 CALHM1, NEURL1-AS1, 6 more genes
    nsv6313941copy number variation1nstd102humanUncertain significance GRCh37 chr10: 105,064,606-105,508,469 , GRCh38.p12 chr10: 103,304,849-103,748,711 CALHM3, NEURL1, 11 more genes
    nsv6131926copy number variation1nstd213human GRCh37 chr10: 103,560,000-105,280,001 , GRCh38.p12 chr10: 101,800,243-103,520,244 ARL3, CYP17A1, 56 more genes
    nsv5635086insertion1nstd207human GRCh38 chr10: 103,475,876-103,475,876 , GRCh37.p13 chr10: 105,235,633-105,235,633 CALHM3
    nsv4974004copy number variation1nstd200human GRCh38 chr10: 103,392,774-103,551,394 , GRCh37.p13 chr10: 105,152,531-105,311,151 MIR1307, NEURL1-AS1, 6 more genes
    nsv4729000copy number variation1nstd102humanUncertain significance GRCh37 chr10: 104,883,845-105,482,700 , GRCh38.p12 chr10: 103,124,088-103,722,942 INA, RNU11-3P, 16 more genes
    nsv4675057copy number variation1nstd102humanUncertain significance GRCh37 chr10: 104,915,576-105,241,844 , GRCh38.p12 chr10: 103,155,819-103,482,087 INA, NT5C2, 13 more genes
    nsv4457357copy number variation1nstd102humanUncertain significance GRCh37 chr10: 104,915,309-105,332,773 , GRCh38.p12 chr10: 103,155,552-103,573,016 PDCD11, TAF5, 14 more genes
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