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Items: 1 to 20 of 951

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098981copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 79,362,452-79,367,880 , GRCh38.p12 chr4: 78,441,298-78,446,726 FRAS1
    nsv7096868copy number variation1nstd102humanUncertain significance GRCh37 chr4: 78,979,164-78,979,259 , GRCh38.p12 chr4: 78,058,010-78,058,105 FRAS1
    nsv7057799inversion1nstd229human GRCh38 chr4: 78,463,095-78,678,686 , GRCh37.p13 chr4: 79,384,249-79,599,840 HIGD1AP13, FRAS1, 2 more genes
    nsv7057586inversion1nstd229human GRCh38 chr4: 78,485,447-78,485,528 , GRCh37.p13 chr4: 79,406,601-79,406,682 FRAS1
    nsv7054052inversion1nstd229human GRCh38 chr4: 78,382,696-78,392,830 , GRCh37.p13 chr4: 79,303,850-79,313,984 FRAS1
    nsv7051354inversion1nstd229human GRCh38 chr4: 78,066,506-78,066,538 , GRCh37.p13 chr4: 78,987,660-78,987,692 LOC107986293, FRAS1
    nsv7050335inversion1nstd229human GRCh38 chr4: 78,386,654-78,392,836 , GRCh37.p13 chr4: 79,307,808-79,313,990 FRAS1
    nsv7049185inversion1nstd229human GRCh38 chr4: 77,808,799-83,184,403 , GRCh37.p13 chr4: 78,729,953-84,105,556 VAMP9P, HNRNPA3P13, 75 more genes
    nsv7048328inversion1nstd229human GRCh38 chr4: 78,051,433-78,061,232 , GRCh37.p13 chr4: 78,972,587-78,982,386 FRAS1
    nsv7045076inversion1nstd229human GRCh38 chr4: 78,485,525-78,485,559 , GRCh37.p13 chr4: 79,406,679-79,406,713 FRAS1
    nsv7045026inversion1nstd229human GRCh38 chr4: 78,252,182-78,252,215 , GRCh37.p13 chr4: 79,173,336-79,173,369 FRAS1
    nsv7043352inversion1nstd229human GRCh38 chr4: 78,414,031-78,414,098 , GRCh37.p13 chr4: 79,335,185-79,335,252 FRAS1
    nsv7040416inversion1nstd229human GRCh38 chr4: 78,147,552-78,271,027 , GRCh37.p13 chr4: 79,068,706-79,192,181 SERBP1P5, FRAS1
    nsv7040415inversion1nstd229human GRCh38 chr4: 72,183,424-80,893,316 , GRCh37.p13 chr4: 73,049,141-81,814,470 , KPNA2P1, 148 more genes
    nsv6757797copy number variation1nstd229human GRCh38 chr4: 78,449,991-78,450,065 , GRCh37.p13 chr4: 79,371,145-79,371,219 FRAS1
    nsv6756397copy number variation1nstd229human GRCh38 chr4: 78,199,401-78,207,500 , GRCh37.p13 chr4: 79,120,555-79,128,654 FRAS1
    nsv6756092copy number variation1nstd229human GRCh38 chr4: 78,377,833-78,379,495 , GRCh37.p13 chr4: 79,298,987-79,300,649 FRAS1, MICOS10P4
    nsv6756041copy number variation1nstd229human GRCh38 chr4: 78,210,022-78,211,853 , GRCh37.p13 chr4: 79,131,176-79,133,007 FRAS1
    nsv6755828copy number variation1nstd229human GRCh38 chr4: 78,049,631-78,061,955 , GRCh37.p13 chr4: 78,970,785-78,983,109 FRAS1
    nsv6754361copy number variation1nstd229human GRCh38 chr4: 78,327,904-78,568,787 , GRCh37.p13 chr4: 79,249,058-79,489,941 FRAS1, ANXA3, 1 more genes
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