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Items: 1 to 20 of 138

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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
    nsv7093855copy number variation1nstd102humanUncertain significance GRCh37 chr10: 102,987,027-103,384,587 , GRCh38.p12 chr10: 101,227,270-101,624,830 RNU2-43P, BTRC, 11 more genes
    nsv7093699copy number variation1nstd102humanUncertain significance GRCh37 chr10: 102,747,968-103,535,657 , GRCh38.p12 chr10: 100,988,211-101,775,900 RNY5P7, TLX1, 25 more genes
    nsv7061391inversion1nstd229human GRCh38 chr10: 100,357,388-105,969,995 , GRCh37.p13 chr10: 102,117,145-107,729,753 , CALHM1, 127 more genes
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6897208copy number variation1nstd229human GRCh38 chr10: 101,621,417-101,623,520 , GRCh37.p13 chr10: 103,381,174-103,383,277 RNU6-1165P, FBXW4
    nsv6891843copy number variation1nstd229human GRCh38 chr10: 101,586,386-101,633,544 , GRCh37.p13 chr10: 103,346,143-103,393,301 FBXW4, MIR3158-1, 4 more genes
    nsv6889052copy number variation1nstd229human GRCh38 chr10: 101,373,162-101,631,853 , GRCh37.p13 chr10: 103,132,919-103,391,610 POLL, RNU6-1165P, 5 more genes
    nsv6883804copy number variation1nstd229human GRCh38 chr10: 101,490,375-101,730,015 , GRCh37.p13 chr10: 103,250,132-103,489,772 , BTRC, 7 more genes
    nsv6880909copy number variation1nstd229human GRCh38 chr10: 101,390,551-101,692,790 , GRCh37.p13 chr10: 103,150,308-103,452,547 FBXW4, MIR3158-1, 5 more genes
    nsv6878686copy number variation1nstd229human GRCh38 chr10: 101,263,286-101,671,540 , GRCh37.p13 chr10: 103,023,043-103,431,297 DPCD, LOC105378453, 9 more genes
    nsv6637358copy number variation1nstd102humanPathogenic GRCh37 chr10: 102,958,930-103,445,585 , GRCh38.p12 chr10: 101,199,173-101,685,828 MIR3158-2, LOC105378453, 11 more genes
    nsv6620151copy number variation1nstd224human GRCh37 chr10: 103,083,978-103,436,164 , GRCh38.p12 chr10: 101,324,221-101,676,407 FBXW4, BTRC, 6 more genes
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6444368copy number variation1nstd223human GRCh38 chr10: 101,432,143-101,672,706 , GRCh37.p13 chr10: 103,191,900-103,432,463 POLL, MIR3158-1, 5 more genes
    nsv6443400copy number variation1nstd223human GRCh38 chr10: 101,310,845-101,668,788 , GRCh37.p13 chr10: 103,070,602-103,428,545 MIR3158-1, FBXW4, 6 more genes
    nsv6309052copy number variation1nstd102humanUncertain significance GRCh37 chr10: 102,987,027-103,530,396 , GRCh38.p12 chr10: 101,227,270-101,770,639 FBXW4, RNU2-59P, 14 more genes
    nsv6131845copy number variation1nstd213human GRCh37 chr10: 100,150,000-103,440,001 , GRCh38.p12 chr10: 98,390,243-101,680,244 CHUK, ABCC2, 70 more genes
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