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Items: 1 to 20 of 502

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140762insertion1nstd232human GRCh37.p13 chr1: 150,406,301-150,406,301 , GRCh38.p12 chr1: 150,433,825-150,433,825 RPRD2
    nsv7099231copy number variation1nstd231human GRCh38.p12 chr1: 149,962,894-151,006,586 , GRCh37 chr1: 149,934,818-150,979,062 ARNT, CTSK, 48 more genes
    nsv7095319copy number variation1nstd102humanUncertain significance GRCh37 chr1: 150,039,915-150,464,158 , GRCh38.p12 chr1: 150,067,858-150,491,682 MIR6878, C1orf54, 15 more genes
    nsv7056211inversion1nstd229human GRCh38 chr1: 143,881,700-152,159,818 , GRCh37.p13 chr1|NW_003871055.3: 697,113-7,283,150 , PDIA3P1, 333 more genes
    nsv7053091inversion1nstd229human GRCh38 chr1: 150,464,714-150,464,765 , GRCh37.p13 chr1|NW_003871055.3: 7,280,127-7,280,178 , GRCh37.p13 chr1: 150,437,190-150,437,241 RPRD2
    nsv7044458inversion1nstd229human GRCh38 chr1: 150,355,899-155,246,175 , GRCh37.p13 chr1: 150,440,214-155,215,966 LCE2C, MUC1, 254 more genes
    nsv7042502inversion1nstd229human GRCh38 chr1: 150,301,267-155,517,761 , GRCh37.p13 chr1: 150,440,214-155,487,552 LINGO4, CELF3, 268 more genes
    nsv6642097copy number variation1nstd229human GRCh38 chr1: 150,390,201-150,404,500 , GRCh37.p13 chr1|NW_003871055.3: 7,205,614-7,219,913 , GRCh37.p13 chr1: 150,362,677-150,376,976 RPRD2
    nsv6642096copy number variation1nstd229human GRCh38 chr1: 150,372,842-150,379,646 , GRCh37.p13 chr1|NW_003871055.3: 7,188,255-7,195,059 , GRCh37.p13 chr1: 150,345,318-150,352,122 RPRD2
    nsv6641916copy number variation1nstd229human GRCh38 chr1: 150,406,738-150,700,622 , GRCh37.p13 chr1: 150,440,214-150,673,098 RNU6-1042P, ENSA, 16 more genes
    nsv6641756copy number variation1nstd229human GRCh38 chr1: 150,433,794-150,433,853 , GRCh37.p13 chr1: 150,406,270-150,406,329 , GRCh37.p13 chr1|NW_003871055.3: 7,249,207-7,249,266 RPRD2
    nsv6641755copy number variation1nstd229human GRCh38 chr1: 150,426,615-150,437,012 , GRCh37.p13 chr1|NW_003871055.3: 7,242,028-7,252,425 , GRCh37.p13 chr1: 150,399,091-150,409,488 RPRD2
    nsv6641662copy number variation1nstd229human GRCh38 chr1: 150,418,789-150,422,056 , GRCh37.p13 chr1|NW_003871055.3: 7,234,202-7,237,469 , GRCh37.p13 chr1: 150,391,265-150,394,532 RPRD2
    nsv6641660copy number variation1nstd229human GRCh38 chr1: 150,379,680-150,382,638 , GRCh37.p13 chr1|NW_003871055.3: 7,195,093-7,198,051 , GRCh37.p13 chr1: 150,352,156-150,355,114 RPRD2
    nsv6641659copy number variation1nstd229human GRCh38 chr1: 150,357,636-150,431,593 , GRCh37.p13 chr1: 150,330,112-150,404,069 , GRCh37.p13 chr1|NW_003871055.3: 7,173,049-7,247,006 RPRD2
    nsv6543423inversion1nstd223human GRCh38 chr1: 150,424,293-150,425,596 , GRCh37.p13 chr1: 150,396,769-150,398,072 , GRCh37.p13 chr1|NW_003871055.3: 7,239,706-7,241,009 RPRD2
    nsv6542370inversion1nstd223human GRCh38 chr1: 150,438,631-150,438,893 , GRCh37.p13 chr1: 150,411,107-150,411,369 , GRCh37.p13 chr1|NW_003871055.3: 7,254,044-7,254,306 RPRD2
    nsv6540461inversion1nstd223human GRCh38 chr1: 150,378,706-150,379,681 , GRCh37.p13 chr1|NW_003871055.3: 7,194,119-7,195,094 , GRCh37.p13 chr1: 150,351,182-150,352,157 RPRD2
    nsv6538572inversion1nstd223human GRCh38 chr1: 150,446,082-150,447,361 , GRCh37.p13 chr1|NW_003871055.3: 7,261,495-7,262,774 , GRCh37.p13 chr1: 150,418,558-150,419,837 RPRD2
    nsv6537973inversion1nstd223human GRCh38 chr1: 150,451,952-150,452,845 , GRCh37.p13 chr1: 150,424,428-150,425,321 , GRCh37.p13 chr1|NW_003871055.3: 7,267,365-7,268,258 RPRD2
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