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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968494inversion1nstd209human GRCh38 chr6: 125,606,968-134,343,905 , GRCh37.p13 chr6: 125,928,114-134,665,043 , ARG1, 137 more genes
    nsv5906945copy number variation1nstd209human GRCh38 chr6: 123,301,756-132,349,395 , GRCh37.p13 chr6: 123,622,901-132,670,534 , LOC105377999, 105 more genes
    nsv5686043mobile element insertion1nstd211human GRCh38 chr6: 130,047,843-130,047,843 , GRCh37.p13 chr6: 130,368,988-130,368,988 L3MBTL3
    nsv5472636copy number variation1nstd206human GRCh38 chr6: 129,669,472-130,238,698 , GRCh37.p13 chr6: 129,990,617-130,559,843 , L3MBTL3, 6 more genes
    nsv5468851copy number variation1nstd206human GRCh38 chr6: 130,056,057-130,056,206 , GRCh37.p13 chr6: 130,377,202-130,377,351 L3MBTL3
    nsv5464824copy number variation1nstd206human GRCh38 chr6: 130,126,134-130,126,200 , GRCh37.p13 chr6: 130,447,279-130,447,345 L3MBTL3
    nsv5409035mobile element insertion1nstd206human GRCh38 chr6: 130,047,843-130,047,894 , GRCh37.p13 chr6: 130,368,988-130,369,039 L3MBTL3
    nsv5363388translocation1nstd200human GRCh38 chr12: 116,738,040-116,738,040 , GRCh38 chr6: 130,121,805-130,121,805 , GRCh37.p13 chr12: 117,175,845-117,175,845 , GRCh37.p13 chr6: 130,442,950-130,442,950 , SPRING1, 2 more genes
    nsv5363387translocation1nstd200human GRCh38 chr10: 94,588,994-94,588,994 , GRCh38 chr6: 130,021,290-130,021,290 , GRCh37.p13 chr10: 96,348,751-96,348,751 , GRCh37.p13 chr6: 130,342,435-130,342,435 HELLS, L3MBTL3
    nsv5117267mobile element insertion1nstd203human GRCh38 chr6: 130,058,149-130,058,176 , GRCh37.p13 chr6: 130,379,294-130,379,321 L3MBTL3
    nsv5109932mobile element insertion1nstd203human GRCh38 chr6: 130,078,973-130,078,985 , GRCh37.p13 chr6: 130,400,118-130,400,130 L3MBTL3
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4934083copy number variation1nstd200human GRCh38 chr6: 130,122,446-130,123,170 , GRCh37.p13 chr6: 130,443,591-130,444,315 L3MBTL3
    nsv4934082copy number variation1nstd200human GRCh38 chr6: 130,057,577-130,057,653 , GRCh37.p13 chr6: 130,378,722-130,378,798 L3MBTL3
    nsv4934081copy number variation1nstd200human GRCh38 chr6: 130,033,413-130,037,105 , GRCh37.p13 chr6: 130,354,558-130,358,250 L3MBTL3
    nsv4826440copy number variation1nstd200human GRCh37 chr6: 130,378,722-130,378,798 , GRCh38.p12 chr6: 130,057,577-130,057,653 L3MBTL3
    nsv4566775mobile element insertion1nstd166human GRCh37.p13 chr6: 130,383,145-130,383,145 , GRCh38.p12 chr6: 130,062,000-130,062,000 L3MBTL3
    nsv4482597mobile element insertion1nstd166human GRCh37.p13 chr6: 130,378,368-130,378,368 , GRCh38.p12 chr6: 130,057,223-130,057,223 L3MBTL3
    nsv4349636copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 129,513,837-132,618,991 , GRCh38.p12 chr6: 129,192,692-132,297,852 ARG1, CCN2, 37 more genes
    nsv4332615sequence alteration1nstd166human GRCh37.p13 chr6: 130,406,799-130,409,309 , GRCh38.p12 chr6: 130,085,654-130,088,164 L3MBTL3
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