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Items: 1 to 20 of 265

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7136948copy number variation1nstd102humanPathogenic GRCh37 chr9: 119,449,661-119,463,580 , GRCh38.p12 chr9: 116,687,382-116,701,301 ASTN2, TRIM32
    nsv7098942copy number variation1nstd102humanUncertain significance GRCh38 chr9: 116,667,613-116,806,157 , GRCh37.p13 chr9: 119,429,892-119,568,436 ASTN2, TRIM32
    nsv7098878copy number variation1nstd102humanPathogenic GRCh37 chr9: 119,448,976-119,461,984 , GRCh38.p12 chr9: 116,686,697-116,699,705 TRIM32, ASTN2
    nsv7098051copy number variation1nstd102humanPathogenic GRCh37 chr9: 119,461,613-119,523,251 , GRCh38.p12 chr9: 116,699,334-116,760,972 ASTN2, TRIM32
    nsv7093122copy number variation1nstd102humanPathogenic GRCh37 chr9: 119,449,580-119,463,580 , GRCh38.p12 chr9: 116,687,301-116,701,301 ASTN2, TRIM32
    nsv6878011copy number variation1nstd229human GRCh38 chr9: 116,677,003-116,711,078 , GRCh37.p13 chr9: 119,439,282-119,473,357 ASTN2, TRIM32
    nsv6876825copy number variation1nstd229human GRCh38 chr9: 116,686,143-116,727,304 , GRCh37.p13 chr9: 119,448,422-119,489,583 ASTN2, TRIM32
    nsv6876382copy number variation1nstd229human GRCh38 chr9: 116,677,056-116,687,142 , GRCh37.p13 chr9: 119,439,335-119,449,421 ASTN2, TRIM32
    nsv6876023copy number variation1nstd229human GRCh38 chr9: 116,691,765-116,736,709 , GRCh37.p13 chr9: 119,454,044-119,498,988 ASTN2, TRIM32
    nsv6874945copy number variation1nstd229human GRCh38 chr9: 116,530,955-116,689,829 , GRCh37.p13 chr9: 119,293,234-119,452,108 ASTN2, ASTN2-AS1, 3 more genes
    nsv6873003copy number variation1nstd229human GRCh38 chr9: 116,668,451-116,707,340 , GRCh37.p13 chr9: 119,430,730-119,469,619 ASTN2, TRIM32
    nsv6872220copy number variation1nstd229human GRCh38 chr9: 116,638,898-116,862,677 , GRCh37.p13 chr9: 119,401,177-119,624,956 ASTN2, LOC105376239, 3 more genes
    nsv6872010copy number variation1nstd229human GRCh38 chr9: 116,657,863-116,697,241 , GRCh37.p13 chr9: 119,420,142-119,459,520 ASTN2, TRIM32
    nsv6870031copy number variation1nstd229human GRCh38 chr9: 116,618,606-116,686,343 , GRCh37.p13 chr9: 119,380,885-119,448,622 ASTN2, TRIM32, 1 more genes
    nsv6869676copy number variation1nstd229human GRCh38 chr9: 116,675,593-116,754,378 , GRCh37.p13 chr9: 119,437,872-119,516,657 TRIM32, ASTN2
    nsv6869633copy number variation1nstd229human GRCh38 chr9: 116,699,959-116,711,592 , GRCh37.p13 chr9: 119,462,238-119,473,871 TRIM32, ASTN2
    nsv6869292copy number variation1nstd229human GRCh38 chr9: 116,660,701-116,691,300 , GRCh37.p13 chr9: 119,422,980-119,453,579 ASTN2, TRIM32
    nsv6868770copy number variation1nstd229human GRCh38 chr9: 116,629,726-116,722,698 , GRCh37.p13 chr9: 119,392,005-119,484,977 ASTN2, TRIM32, 1 more genes
    nsv6868586copy number variation1nstd229human GRCh38 chr9: 116,644,280-116,706,143 , GRCh37.p13 chr9: 119,406,559-119,468,422 TRIM32, LOC105376240, 1 more genes
    nsv6868191copy number variation1nstd229human GRCh38 chr9: 116,688,489-116,706,250 , GRCh37.p13 chr9: 119,450,768-119,468,529 ASTN2, TRIM32
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