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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6114689mobile element insertion1nstd186human GRCh37 chr12: 126,953,871-126,953,922 , GRCh38.p12 chr12: 126,469,325-126,469,376 LINC02347
    nsv5969216insertion1nstd209human GRCh38 chr12: 126,469,311-126,469,311 , GRCh37.p13 chr12: 126,953,857-126,953,857 LINC02347
    nsv5940039copy number variation1nstd209human GRCh38 chr12: 126,443,119-126,443,179 , GRCh37.p13 chr12: 126,927,665-126,927,725 LINC02825, LINC02347
    nsv5700377mobile element insertion2nstd211human GRCh38 chr12: 126,469,325-126,469,325 , GRCh37.p13 chr12: 126,953,871-126,953,871 LINC02347
    nsv5647193insertion1nstd207human GRCh38 chr12: 126,469,311-126,469,311 , GRCh37.p13 chr12: 126,953,857-126,953,857 LINC02347
    nsv5511207copy number variation1nstd206human GRCh38 chr12: 126,159,513-126,449,586 , GRCh37.p13 chr12: 126,644,059-126,934,132 , LINC02825, 7 more genes
    nsv5497473copy number variation1nstd206human GRCh38 chr12: 126,251,831-127,523,787 , GRCh37.p13 chr12: 126,736,377-128,008,332 RNU1-104P, LOC121296, 28 more genes
    nsv5495170copy number variation1nstd206human GRCh38 chr12: 126,463,767-126,616,017 , GRCh37.p13 chr12: 126,948,313-127,100,563 NDUFA5P6, LOC100421201, 2 more genes
    nsv5429131mobile element insertion1nstd206human GRCh38 chr12: 126,469,325-126,469,376 , GRCh37.p13 chr12: 126,953,871-126,953,922 LINC02347
    nsv5383280mobile element deletion1nstd186human GRCh37 chr12: 126,926,486-126,926,788 , GRCh38.p12 chr12: 126,441,940-126,442,242 LINC02825, LINC02347
    nsv5333346translocation1nstd200human GRCh37 chr12: 126,927,726-126,927,726 , GRCh37 chr12: 126,927,669-126,927,669 , GRCh38.p12 chr12: 126,443,123-126,443,123 , GRCh38.p12 chr12: 126,443,180-126,443,180 LINC02347, LINC02825
    nsv5130676mobile element insertion1nstd203human GRCh38 chr12: 126,469,313-126,469,325 , GRCh37.p13 chr12: 126,953,859-126,953,871 LINC02347
    nsv5130185mobile element insertion1nstd203human GRCh38 chr12: 126,469,311-126,469,325 , GRCh37.p13 chr12: 126,953,857-126,953,871 LINC02347
    nsv5124317mobile element insertion1nstd203human GRCh38 chr12: 126,469,312-126,469,325 , GRCh37.p13 chr12: 126,953,858-126,953,871 LINC02347
    nsv5123813mobile element insertion1nstd203human GRCh38 chr12: 126,469,315-126,469,325 , GRCh37.p13 chr12: 126,953,861-126,953,871 LINC02347
    nsv5121820mobile element insertion1nstd203human GRCh38 chr12: 126,469,316-126,469,325 , GRCh37.p13 chr12: 126,953,862-126,953,871 LINC02347
    nsv4996282copy number variation1nstd200human GRCh38 chr12: 126,066,300-126,503,199 , GRCh37.p13 chr12: 126,550,846-126,987,745 , LINC02350, 9 more genes
    nsv4993852copy number variation1nstd200human GRCh38 chr12: 126,460,634-126,461,478 , GRCh37.p13 chr12: 126,945,180-126,946,024 LINC02347
    nsv4993850copy number variation1nstd200human GRCh38 chr12: 126,389,353-126,747,623 , GRCh37.p13 chr12: 126,873,899-127,232,169 LINC00944, LOC107984448, 10 more genes
    nsv4899842mobile element deletion1nstd200human GRCh38 chr12: 126,441,940-126,442,242 , GRCh37.p13 chr12: 126,926,486-126,926,788 LINC02825, LINC02347
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