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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977361inversion1nstd209human GRCh38 chr7: 5,132,403-5,833,612 , GRCh37.p13 chr7: 5,172,034-5,873,243 , ACTB, 15 more genes
    nsv5914961copy number variation1nstd209human GRCh38 chr7: 5,213,104-5,213,162 , GRCh37.p13 chr7: 5,252,735-5,252,793 WIPI2
    nsv5562206sequence alteration1nstd206human GRCh38 chr7: 4,983,711-5,730,820 , GRCh37.p13 chr7: 5,023,342-5,770,451 , FSCN1, 21 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5554692sequence alteration1nstd206human GRCh38 chr7: 5,142,858-5,773,733 , GRCh37.p13 chr7: 5,182,489-5,813,364 , FSCN1, 14 more genes
    nsv5552490insertion1nstd206human GRCh38 chr7: 5,202,597-5,202,647 , GRCh37.p13 chr7: 5,242,228-5,242,278 WIPI2
    nsv5470865copy number variation1nstd206human GRCh38 chr7: 5,207,577-5,207,760 , GRCh37.p13 chr7: 5,247,208-5,247,391 WIPI2
    nsv5468391copy number variation1nstd206human GRCh38 chr7: 5,184,568-5,188,742 , GRCh37.p13 chr7: 5,224,199-5,228,373 WIPI2
    nsv5458587copy number variation1nstd206human GRCh38 chr7: 5,213,110-5,213,163 , GRCh37.p13 chr7: 5,252,741-5,252,794 WIPI2
    nsv5370141translocation1nstd200human GRCh38 chr7: 5,201,021-5,201,021 , GRCh38 chr7: 5,200,925-5,200,925 , GRCh37.p13 chr7: 5,240,556-5,240,556 , GRCh37.p13 chr7: 5,240,652-5,240,652 WIPI2
    nsv5235653copy number variation1nstd204human GRCh37.p13 chr7: 5,239,332-5,603,931 , GRCh38.p13 chr7: 5,199,701-5,564,300 ACTB, WIPI2, 7 more genes
    nsv4953283copy number variation1nstd200human GRCh38 chr7: 5,207,577-5,207,760 , GRCh37.p13 chr7: 5,247,208-5,247,391 WIPI2
    nsv4949891copy number variation1nstd200human GRCh38 chr7: 5,186,146-5,191,189 , GRCh37.p13 chr7: 5,225,777-5,230,820 WIPI2
    nsv4825013copy number variation1nstd200human GRCh37 chr7: 5,247,208-5,247,391 , GRCh38.p12 chr7: 5,207,577-5,207,760 WIPI2
    nsv4818547copy number variation1nstd200human GRCh37 chr7: 5,254,803-5,255,422 , GRCh38.p12 chr7: 5,215,172-5,215,791 WIPI2
    nsv4818546copy number variation1nstd200human GRCh37 chr7: 5,240,556-5,240,652 , GRCh38.p12 chr7: 5,200,925-5,201,021 WIPI2
    nsv4818545copy number variation1nstd200human GRCh37 chr7: 5,235,493-5,236,481 , GRCh38.p12 chr7: 5,195,862-5,196,850 WIPI2
    nsv4818544copy number variation1nstd200human GRCh37 chr7: 5,225,777-5,230,820 , GRCh38.p12 chr7: 5,186,146-5,191,189 WIPI2
    nsv4818543copy number variation1nstd200human GRCh37 chr7: 5,224,206-5,228,247 , GRCh38.p12 chr7: 5,184,575-5,188,616 WIPI2
    nsv4729601copy number variation1nstd102humanUncertain significance GRCh37 chr7: 5,132,817-5,284,485 , GRCh38.p12 chr7: 5,093,186-5,244,854 ZNF890P, OR10AH1P, 2 more genes
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