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Items: 1 to 20 of 145

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096799copy number variation1nstd102humanUncertain significance GRCh37 chr3: 38,180,153-38,618,292 , GRCh38.p12 chr3: 38,138,662-38,576,801 ACVR2B-AS1, SCN5A, 13 more genes
    nsv7096465copy number variation1nstd102humanUncertain significance GRCh37 chr3: 38,495,814-38,991,853 , GRCh38.p12 chr3: 38,454,323-38,950,362 ACVR2B, LOC107986042, 8 more genes
    nsv7056165inversion1nstd229human GRCh38 chr3: 38,502,176-38,676,239 , GRCh37.p13 chr3: 38,543,667-38,717,730 SCN5A, RPL18AP7, 2 more genes
    nsv7051268inversion1nstd229human GRCh38 chr3: 37,000,362-39,352,689 , GRCh37.p13 chr3: 37,041,853-39,394,180 PLCD1, RNU6-1227P, 59 more genes
    nsv7048850inversion1nstd229human GRCh38 chr3: 37,408,411-39,634,596 , GRCh37.p13 chr3: 37,449,902-39,676,087 OXSR1, ITGA9, 55 more genes
    nsv7042103inversion1nstd229human GRCh38 chr3: 37,827,304-38,566,908 , GRCh37.p13 chr3: 37,868,795-38,608,399 SCN5A, CDC42P7, 22 more genes
    nsv7039010inversion1nstd229human GRCh38 chr3: 37,851,228-39,078,678 , GRCh37.p13 chr3: 37,892,719-39,120,169 CDC42P7, LOC105377033, 28 more genes
    nsv6715860copy number variation1nstd229human GRCh38 chr3: 38,523,288-38,657,754 , GRCh37.p13 chr3: 38,564,779-38,699,245 RPL18AP7, EXOG, 1 more genes
    nsv6700406copy number variation1nstd229human GRCh38 chr3: 38,505,701-38,507,881 , GRCh37.p13 chr3: 38,547,192-38,549,372 EXOG
    nsv6537958inversion1nstd223human GRCh38 chr3: 37,408,438-39,634,613 , GRCh37.p13 chr3: 37,449,929-39,676,104 ITGA9-AS1, MIR26A1, 55 more genes
    nsv6363638copy number variation1nstd223human GRCh38 chr3: 38,502,175-38,504,605 , GRCh37.p13 chr3: 38,543,666-38,546,096 EXOG
    nsv6313749copy number variation1nstd102humanUncertain significance GRCh37 chr3: 38,566,234-38,698,720 , GRCh38.p12 chr3: 38,524,743-38,657,229 RPL18AP7, SCN5A, 1 more genes
    nsv6313737copy number variation1nstd102humanUncertain significance GRCh37 chr3: 38,109,534-38,669,316 , GRCh38.p12 chr3: 38,068,043-38,627,825 ACVR2B-AS1, SCN5A, 16 more genes
    nsv6311982copy number variation1nstd102humanUncertain significance GRCh37 chr3: 37,034,542-38,835,501 , GRCh38.p12 chr3: 36,993,051-38,794,010 SCN10A, PPP2R2DP1, 41 more genes
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 LOC102724104, CRIP1P2, 291 more genes
    nsv6293418mobile element insertion1nstd186human GRCh37 chr3: 38,541,650-38,541,701 , GRCh38.p12 chr3: 38,500,159-38,500,210 EXOG
    nsv6253892mobile element insertion1nstd215human GRCh38 chr3: 38,514,775-38,514,775 , GRCh37.p13 chr3: 38,556,266-38,556,266 EXOG, DDTP1
    nsv5993830copy number variation1nstd212human GRCh38 chr3: 38,502,010-38,504,403 , GRCh37.p13 chr3: 38,543,501-38,545,894 EXOG
    nsv5905725copy number variation1nstd209human GRCh38 chr3: 38,519,237-38,520,432 , GRCh37.p13 chr3: 38,560,728-38,561,923 EXOG
    nsv5693465mobile element insertion2nstd211human GRCh38 chr3: 38,500,159-38,500,159 , GRCh37.p13 chr3: 38,541,650-38,541,650 EXOG
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