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Items: 1 to 20 of 237

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5931438copy number variation1nstd209human GRCh38 chr12: 122,525,791-122,526,119 , GRCh37.p13 chr12: 123,010,338-123,010,666 RSRC2, KNTC1
    nsv5708101mobile element insertion1nstd211human GRCh38 chr12: 122,504,161-122,504,161 , GRCh37.p13 chr12: 122,988,708-122,988,708 RSRC2
    nsv5588065copy number variation1nstd207human GRCh38 chr12: 122,525,791-122,526,119 , GRCh37.p13 chr12: 123,010,338-123,010,666 KNTC1, RSRC2
    nsv5506821copy number variation1nstd206human GRCh38 chr12: 122,525,799-122,526,120 , GRCh37.p13 chr12: 123,010,346-123,010,667 KNTC1, RSRC2
    nsv5433890mobile element insertion1nstd206human GRCh38 chr12: 122,504,161-122,504,212 , GRCh37.p13 chr12: 122,988,708-122,988,759 RSRC2
    nsv5382369mobile element deletion2nstd186human GRCh37 chr12: 123,010,346-123,010,667 , GRCh38.p12 chr12: 122,525,799-122,526,120 RSRC2, KNTC1
    nsv5374063translocation1nstd200human GRCh38 chr12: 122,506,640-122,506,640 , GRCh38 chr12: 122,498,337-122,498,337 , GRCh37.p13 chr12: 122,991,187-122,991,187 , GRCh37.p13 chr12: 122,982,884-122,982,884 ZCCHC8, RSRC2
    nsv5313400copy number variation1nstd204human GRCh38.p13 chr12: 122,498,327-122,506,648 , GRCh37.p13 chr12: 122,982,874-122,991,195 ZCCHC8, RSRC2
    nsv5278737copy number variation1nstd204human GRCh38.p13 chr12: 122,498,201-122,505,900 , GRCh37.p13 chr12: 122,982,748-122,990,447 ZCCHC8, RSRC2
    nsv5276873copy number variation1nstd204human GRCh38.p13 chr12: 122,498,375-122,506,738 , GRCh37.p13 chr12: 122,982,922-122,991,285 RSRC2, ZCCHC8
    nsv5275241copy number variation1nstd204human GRCh38.p13 chr12: 122,493,201-122,521,600 , GRCh37.p13 chr12: 122,977,748-123,006,147 ZCCHC8, RSRC2
    nsv5271531copy number variation1nstd204human GRCh38.p13 chr12: 122,467,401-122,526,100 , GRCh37.p13 chr12: 122,951,948-123,010,647 KNTC1, RSRC2, 1 more genes
    nsv5270419copy number variation1nstd204human GRCh38.p13 chr12: 122,494,683-122,512,161 , GRCh37.p13 chr12: 122,979,230-122,996,708 RSRC2, ZCCHC8
    nsv5205376mobile element deletion1nstd204human GRCh37.p13 chr12: 123,010,346-123,010,667 , GRCh38.p13 chr12: 122,525,799-122,526,120 RSRC2, KNTC1
    nsv4899840mobile element deletion1nstd200human GRCh38 chr12: 122,525,799-122,526,120 , GRCh37.p13 chr12: 123,010,346-123,010,667 RSRC2, KNTC1
    nsv4832429copy number variation1nstd200human GRCh37 chr12: 122,982,884-122,991,188 , GRCh38.p12 chr12: 122,498,337-122,506,641 ZCCHC8, RSRC2
    nsv4775177mobile element deletion1nstd200human GRCh37 chr12: 123,010,346-123,010,667 , GRCh38.p12 chr12: 122,525,799-122,526,120 RSRC2, KNTC1
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
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