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Items: 1 to 20 of 941

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142547copy number variation1nstd232human GRCh37.p13 chr1: 1,231,730-1,231,782 , GRCh38.p12 chr1: 1,296,350-1,296,402 ACAP3, MIR6726
    nsv7137045copy number variation1nstd102humanPathogenic GRCh37 chr1: 536,777-6,012,896 , GRCh38.p12 chr1: 601,397-5,952,836 MIR200B, LOC105378608, 172 more genes
    nsv7099018copy number variation1nstd102humanPathogenic GRCh37 chr1: 1-2,580,976 , GRCh38.p12 chr1: 10,001-2,649,537 DVL1, LOC100129534, 148 more genes
    nsv7047478inversion1nstd229human GRCh38 chr1: 1,251,496-1,290,408 , GRCh37.p13 chr1: 1,186,876-1,225,788 LINC01786, ACAP3, 2 more genes
    nsv7044349inversion1nstd229human GRCh38 chr1: 1,282,566-1,352,764 , GRCh37.p13 chr1: 1,217,946-1,288,144 PUSL1, MIR6808, 10 more genes
    nsv7044270inversion1nstd229human GRCh38 chr1: 1,133,718-2,842,494 , GRCh37.p13 chr1: 1,069,098-2,759,059 LOC105378586, MIR6726, 91 more genes
    nsv7042361inversion1nstd229human GRCh38 chr1: 1,275,702-1,304,338 , GRCh37.p13 chr1: 1,211,082-1,239,718 LINC01786, MIR6726, 3 more genes
    nsv6641147copy number variation1nstd229human GRCh38 chr1: 1,274,039-1,295,942 , GRCh37.p13 chr1: 1,209,419-1,231,322 ACAP3, LINC01786, 3 more genes
    nsv6641066copy number variation1nstd229human GRCh38 chr1: 1,299,401-1,301,100 , GRCh37.p13 chr1: 1,234,781-1,236,480 ACAP3
    nsv6640543copy number variation1nstd229human GRCh38 chr1: 1,156,215-1,304,768 , GRCh37.p13 chr1: 1,091,595-1,240,148 MIR429, TTLL10, 14 more genes
    nsv6639644copy number variation1nstd229human GRCh38 chr1: 1,089,392-1,302,400 , GRCh37.p13 chr1: 1,024,772-1,237,780 B3GALT6, C1QTNF12, 15 more genes
    nsv6637093copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897 VWA1, CEP104, 311 more genes
    nsv6637018copy number variation1nstd102humanUncertain significance GRCh37 chr1: 1,129,319-1,264,880 , GRCh38.p12 chr1: 1,193,939-1,329,500 SNORD167, TAS1R3, 15 more genes
    nsv6636661copy number variation1nstd102humanUncertain significance GRCh37 chr1: 1,130,311-2,397,177 , GRCh38.p12 chr1: 1,194,931-2,465,738 ATAD3C, ACAP3, 69 more genes
    nsv6636292copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-2,972,435 , GRCh38.p12 chr1: 914,087-3,055,871 LOC105378602, LOC105378599, 108 more genes
    nsv6635030copy number variation1nstd227human GRCh38.p12 chr1: 1,303,959-1,311,592 , GRCh37 chr1: 1,239,339-1,246,972 INTS11, ACAP3, 3 more genes
    nsv6625736copy number variation2nstd224human GRCh37 chr1: 1,222,895-1,244,646 , GRCh38.p12 chr1: 1,287,515-1,309,266 PUSL1, MIR6726, 3 more genes
    nsv6625735copy number variation2nstd224human GRCh37 chr1: 1,220,954-1,244,646 , GRCh38.p12 chr1: 1,285,574-1,309,266 SCNN1D, ACAP3, 3 more genes
    nsv6625602copy number variation1nstd224human GRCh37 chr1: 1,226,757-1,268,687 , GRCh38.p12 chr1: 1,291,377-1,333,307 TAS1R3, ACAP3, 8 more genes
    nsv6625601copy number variation1nstd224human GRCh37 chr1: 1,222,958-1,244,646 , GRCh38.p12 chr1: 1,287,578-1,309,266 SCNN1D, PUSL1, 3 more genes
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