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Items: 1 to 20 of 515

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098987copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 97,873,920-97,887,367 , GRCh38.p12 chr9: 95,111,638-95,125,085 FANCC, AOPEP, 1 more genes
    nsv7097970copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,897,618-97,912,379 , GRCh38.p12 chr9: 95,135,336-95,150,097 FANCC, RNA5SP288, 1 more genes
    nsv7077729inversion1nstd229human GRCh38 chr9: 94,417,509-96,970,614 , GRCh37.p13 chr9: 97,179,791-99,732,896 HSD17B3-AS1, ERCC6L2, 60 more genes
    nsv7075365inversion1nstd229human GRCh38 chr9: 94,549,389-100,549,990 , GRCh37.p13 chr9: 97,311,671-103,312,272 PCAT7, ANKS6, 128 more genes
    nsv7065950inversion1nstd229human GRCh38 chr9: 95,084,728-95,254,679 , GRCh37.p13 chr9: 97,847,010-98,016,961 AOPEP, MIR24-1, 7 more genes
    nsv7062884inversion1nstd229human GRCh38 chr9: 95,132,376-95,136,733 , GRCh37.p13 chr9: 97,894,658-97,899,015 FANCC, AOPEP
    nsv7061823inversion1nstd229human GRCh38 chr9: 94,710,575-96,645,135 , GRCh37.p13 chr9: 97,472,857-99,407,417 LOC105376163, LINC00092, 42 more genes
    nsv6875836copy number variation1nstd229human GRCh38 chr9: 95,139,825-95,141,989 , GRCh37.p13 chr9: 97,902,107-97,904,271 FANCC, AOPEP, 1 more genes
    nsv6875276copy number variation1nstd229human GRCh38 chr9: 95,299,301-95,303,300 , GRCh37.p13 chr9: 98,061,583-98,065,582 FANCC
    nsv6873287copy number variation1nstd229human GRCh38 chr9: 95,204,370-95,205,038 , GRCh37.p13 chr9: 97,966,652-97,967,320 FANCC
    nsv6872628copy number variation1nstd229human GRCh38 chr9: 94,768,901-95,577,300 , GRCh37.p13 chr9: 97,531,183-98,339,582 RPS26P37, MIR27B, 17 more genes
    nsv6872262copy number variation1nstd229human GRCh38 chr9: 95,140,201-95,155,500 , GRCh37.p13 chr9: 97,902,483-97,917,782 FANCC, RNA5SP288, 1 more genes
    nsv6870542copy number variation1nstd229human GRCh38 chr9: 95,132,501-95,139,400 , GRCh37.p13 chr9: 97,894,783-97,901,682 AOPEP, FANCC
    nsv6869093copy number variation1nstd229human GRCh38 chr9: 95,231,152-95,243,012 , GRCh37.p13 chr9: 97,993,434-98,005,294 FANCC
    nsv6868657copy number variation1nstd229human GRCh38 chr9: 95,202,506-95,202,898 , GRCh37.p13 chr9: 97,964,788-97,965,180 FANCC
    nsv6868146copy number variation1nstd229human GRCh38 chr9: 95,125,751-95,126,196 , GRCh37.p13 chr9: 97,888,033-97,888,478 AOPEP, FANCC
    nsv6867729copy number variation1nstd229human GRCh38 chr9: 95,167,509-95,204,776 , GRCh37.p13 chr9: 97,929,791-97,967,058 FANCC
    nsv6867485copy number variation1nstd229human GRCh38 chr9: 95,149,686-95,229,204 , GRCh37.p13 chr9: 97,911,968-97,991,486 FANCC
    nsv6866786copy number variation1nstd229human GRCh38 chr9: 95,308,881-95,311,142 , GRCh37.p13 chr9: 98,071,163-98,073,424 FANCC
    nsv6863654copy number variation1nstd229human GRCh38 chr9: 95,227,039-95,227,504 , GRCh37.p13 chr9: 97,989,321-97,989,786 FANCC
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