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Items: 1 to 20 of 230

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112763copy number variation1nstd102humanPathogenic GRCh37 chr12: 189,145-7,730,395 , GRCh38.p12 chr12: 79,979-7,577,799 GALNT8, LINC02371, 197 more genes
    nsv5921785copy number variation1nstd209human GRCh38 chr12: 6,360,348-6,360,429 , GRCh37.p13 chr12: 6,469,514-6,469,595 SCNN1A
    nsv5916628copy number variation1nstd209human GRCh38 chr12: 6,369,294-6,369,362 , GRCh37.p13 chr12: 6,478,460-6,478,528 LOC105369626, SCNN1A
    nsv5719013mobile element insertion1nstd211human GRCh38 chr12: 6,358,267-6,358,267 , GRCh37.p13 chr12: 6,467,433-6,467,433 SCNN1A
    nsv5663989insertion1nstd207human GRCh38 chr12: 6,369,365-6,369,365 , GRCh37.p13 chr12: 6,478,531-6,478,531 LOC105369626, SCNN1A
    nsv5657165insertion1nstd207human GRCh38 chr12: 6,362,935-6,362,935 , GRCh37.p13 chr12: 6,472,101-6,472,101 SCNN1A
    nsv5653763insertion1nstd207human GRCh38 chr12: 6,369,294-6,369,294 , GRCh37.p13 chr12: 6,478,460-6,478,460 LOC105369626, SCNN1A
    nsv5564211copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,438,478-7,362,819 , GRCh38.p12 chr12: 6,329,312-7,210,223 GPR162, SCARNA11, 68 more genes
    nsv5556209mobile element insertion1nstd206human GRCh38 chr12: 6,358,267-6,358,318 , GRCh37.p13 chr12: 6,467,433-6,467,484 SCNN1A
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5313887copy number variation1nstd204human GRCh37.p13 chr12: 6,459,161-6,462,971 , GRCh38.p13 chr12: 6,349,995-6,353,805 SCNN1A, LOC107984500
    nsv5279219copy number variation1nstd204human GRCh38.p13 chr12: 6,349,776-6,353,865 , GRCh37.p13 chr12: 6,458,942-6,463,031 SCNN1A, LOC107984500
    nsv5191213mobile element insertion1nstd203human GRCh38 chr12: 6,345,171-6,345,183 , GRCh37.p13 chr12: 6,454,337-6,454,349 SCNN1A, RN7SL391P, 1 more genes
    nsv5139156mobile element insertion1nstd203human GRCh38 chr12: 6,362,938-6,362,962 , GRCh37.p13 chr12: 6,472,104-6,472,128 SCNN1A
    nsv5137587mobile element insertion1nstd203human GRCh38 chr12: 6,353,641-6,353,691 , GRCh37.p13 chr12: 6,462,807-6,462,857 LOC107984500, SCNN1A
    nsv5137341mobile element insertion1nstd203human GRCh38 chr12: 6,353,685-6,353,691 , GRCh37.p13 chr12: 6,462,851-6,462,857 SCNN1A, LOC107984500
    nsv5136394mobile element insertion1nstd203human GRCh38 chr12: 6,353,691-6,353,732 , GRCh37.p13 chr12: 6,462,857-6,462,898 SCNN1A, LOC107984500
    nsv5136206mobile element insertion1nstd203human GRCh38 chr12: 6,353,672-6,353,691 , GRCh37.p13 chr12: 6,462,838-6,462,857 SCNN1A, LOC107984500
    nsv5134564mobile element insertion1nstd203human GRCh38 chr12: 6,353,640-6,353,691 , GRCh37.p13 chr12: 6,462,806-6,462,857 LOC107984500, SCNN1A
    nsv5133692mobile element insertion1nstd203human GRCh38 chr12: 6,362,898-6,362,935 , GRCh37.p13 chr12: 6,472,064-6,472,101 SCNN1A
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