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Items: 1 to 20 of 577

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5706686mobile element insertion1nstd211human GRCh38 chr9: 136,670,707-136,670,707 , GRCh37.p13 chr9: 139,565,159-139,565,159 MIR126, EGFL7
    nsv5699503mobile element insertion1nstd211human GRCh38 chr9: 136,662,905-136,662,905 , GRCh37.p13 chr9: 139,557,357-139,557,357 EGFL7
    nsv5587827copy number variation1nstd207human GRCh38 chr9: 136,671,235-136,671,286 , GRCh37.p13 chr9: 139,565,687-139,565,738 EGFL7, AGPAT2
    nsv5564455copy number variation1nstd102humanUncertain significance GRCh37 chr9: 139,297,240-139,572,028 , GRCh38.p12 chr9: 136,402,788-136,677,576 LOC105376325, NOTCH1, 14 more genes
    nsv5489359copy number variation1nstd206human GRCh38 chr9: 136,672,589-136,673,269 , GRCh37.p13 chr9: 139,567,041-139,567,721 AGPAT2, EGFL7
    nsv5483599copy number variation1nstd206human GRCh38 chr9: 136,662,679-136,662,732 , GRCh37.p13 chr9: 139,557,131-139,557,184 EGFL7
    nsv5481176copy number variation1nstd206human GRCh38 chr9: 136,652,303-136,655,003 , GRCh37.p13 chr9: 139,546,755-139,549,455 LOC102724193, HSPC324, 1 more genes
    nsv5411277mobile element insertion1nstd206human GRCh38 chr9: 136,670,707-136,670,758 , GRCh37.p13 chr9: 139,565,159-139,565,210 MIR126, EGFL7
    nsv5410721mobile element insertion1nstd206human GRCh38 chr9: 136,662,905-136,662,956 , GRCh37.p13 chr9: 139,557,357-139,557,408 EGFL7
    nsv5381762copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,284,464-141,018,984 , GRCh38.p12 chr9: 136,390,012-138,124,532 ARRDC1, SETP5, 101 more genes
    nsv5248645copy number variation1nstd204human GRCh38.p13 chr9: 136,668,964-136,672,263 , GRCh37.p13 chr9: 139,563,416-139,566,715 MIR126, AGPAT2, 1 more genes
    nsv5246206copy number variation1nstd204human GRCh38.p13 chr9: 136,043,001-136,766,200 , GRCh37.p13 chr9: 138,934,847-139,660,652 MIR4674, TMEM250, 37 more genes
    nsv5242695copy number variation1nstd204human GRCh38.p13 chr9: 136,672,990-136,682,707 , GRCh37.p13 chr9: 139,567,442-139,577,159 AGPAT2, EGFL7
    nsv4985870copy number variation1nstd200human GRCh38 chr9: 136,632,294-136,850,190 , GRCh37.p13 chr9: 139,526,746-139,744,642 CCDC183, PHPT1, 25 more genes
    nsv4985869copy number variation1nstd200human GRCh38 chr9: 136,591,087-136,947,348 , GRCh37.p13 chr9: 139,485,539-139,841,800 LOC102724193, AJM1, 34 more genes
    nsv4985868copy number variation1nstd200human GRCh38 chr9: 136,528,503-136,809,431 , GRCh37.p13 chr9: 139,422,955-139,703,883 LCN6, DIPK1B, 25 more genes
    nsv4973368copy number variation1nstd200human GRCh38 chr9: 136,672,589-136,673,269 , GRCh37.p13 chr9: 139,567,041-139,567,721 EGFL7, AGPAT2
    nsv4973367copy number variation1nstd200human GRCh38 chr9: 136,656,458-136,657,514 , GRCh37.p13 chr9: 139,550,910-139,551,966 EGFL7, HSPC324
    nsv4973366copy number variation1nstd200human GRCh38 chr9: 136,652,603-136,654,492 , GRCh37.p13 chr9: 139,547,055-139,548,944 LOC102724193, HSPC324, 1 more genes
    nsv4845671copy number variation1nstd200human GRCh37 chr9: 139,422,955-139,703,883 , GRCh38.p12 chr9: 136,528,503-136,809,431 TMEM141, CCDC183, 25 more genes
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