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Items: 1 to 20 of 284

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7096531copy number variation1nstd102humanUncertain significance GRCh37 chr3: 121,489,192-125,313,644 , GRCh38.p12 chr3: 121,770,345-125,594,800 MEMO1P6, HACD2, 62 more genes
    nsv6717928copy number variation1nstd229human GRCh38 chr3: 122,561,318-123,338,455 , GRCh37.p13 chr3: 122,280,165-123,057,302 PARP15, HSPBAP1, 12 more genes
    nsv6715423copy number variation1nstd229human GRCh38 chr3: 123,136,009-123,143,818 , GRCh37.p13 chr3: 122,854,856-122,862,665 PDIA5
    nsv6706075copy number variation1nstd229human GRCh38 chr3: 123,068,038-123,068,149 , GRCh37.p13 chr3: 122,786,885-122,786,996 PDIA5
    nsv6704766copy number variation1nstd229human GRCh38 chr3: 123,079,195-123,079,538 , GRCh37.p13 chr3: 122,798,042-122,798,385 PDIA5
    nsv6703931copy number variation1nstd229human GRCh38 chr3: 118,573,267-126,079,281 , GRCh37.p13 chr3: 118,292,114-125,798,124 RPS24P9, LOC105374064, 149 more genes
    nsv6702801copy number variation1nstd229human GRCh38 chr3: 123,141,471-123,143,790 , GRCh37.p13 chr3: 122,860,318-122,862,637 PDIA5
    nsv6701823copy number variation1nstd229human GRCh38 chr3: 123,135,698-123,138,115 , GRCh37.p13 chr3: 122,854,545-122,856,962 PDIA5
    nsv6701217copy number variation1nstd229human GRCh38 chr3: 123,141,557-123,141,650 , GRCh37.p13 chr3: 122,860,404-122,860,497 PDIA5
    nsv6698694copy number variation1nstd229human GRCh38 chr3: 123,150,401-123,264,700 , GRCh37.p13 chr3: 122,869,248-122,983,547 SEC22A, PDIA5, 1 more genes
    nsv6698511copy number variation1nstd229human GRCh38 chr3: 123,112,203-123,114,482 , GRCh37.p13 chr3: 122,831,050-122,833,329 PDIA5
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6556022inversion1nstd223human GRCh38 chr3: 123,151,729-129,172,574 , GRCh37.p13 chr3: 122,870,576-128,891,417 UMPS, CHST13, 139 more genes
    nsv6373184copy number variation1nstd223human GRCh38 chr3: 123,135,698-123,138,113 , GRCh37.p13 chr3: 122,854,545-122,856,960 PDIA5
    nsv6315285copy number variation1nstd102humanUncertain significance GRCh38 chr3: 122,157,406-123,113,479 , GRCh37.p13 chr3: 121,876,253-122,832,326 SEMA5B, EIF4BP8, 19 more genes
    nsv6311770copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,365,818-133,465,047 , GRCh38.p12 chr3: 120,646,971-133,746,203 HNRNPA1P23, MIX23, 278 more genes
    nsv6293404mobile element insertion1nstd186human GRCh37 chr3: 122,799,753-122,799,804 , GRCh38.p12 chr3: 123,080,906-123,080,957 PDIA5
    nsv6278803insertion1nstd214human GRCh38 chr3: 123,151,874-123,151,874 , GRCh37.p13 chr3: 122,870,721-122,870,721 PDIA5
    nsv6254623mobile element insertion1nstd215human GRCh38 chr3: 123,080,906-123,080,906 , GRCh37.p13 chr3: 122,799,753-122,799,753 PDIA5
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