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Items: 1 to 20 of 265

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094203copy number variation1nstd102humanUncertain significance GRCh37 chr12: 122,277,634-124,242,579 , GRCh38.p12 chr12: 121,839,728-123,758,032 SBNO1, MIR9902-1, 58 more genes
    nsv7094033copy number variation1nstd102humanUncertain significance GRCh37 chr12: 124,116,872-124,118,104 , GRCh38.p12 chr12: 123,632,325-123,633,557 GTF2H3, EIF2B1
    nsv7074643inversion1nstd229human GRCh38 chr12: 123,471,880-125,706,144 , GRCh37.p13 chr12: 123,956,427-126,190,690 DHX37, RNU6-927P, 44 more genes
    nsv7074199inversion1nstd229human GRCh38 chr12: 123,186,434-132,825,682 , GRCh37.p13 chr12: 123,670,981-133,402,268 PIWIL1, FZD10-AS1, 187 more genes
    nsv7071183inversion1nstd229human GRCh38 chr12: 122,804,561-124,735,813 , GRCh37.p13 chr12: 123,289,108-125,220,359 TMED2, GTF2H3, 41 more genes
    nsv7063627inversion1nstd229human GRCh38 chr12: 123,448,954-124,156,419 , GRCh37.p13 chr12: 123,933,501-124,640,965 ZNF664, CCDC92, 17 more genes
    nsv7060836inversion1nstd229human GRCh38 chr12: 123,595,397-123,673,541 , GRCh37.p13 chr12: 124,079,944-124,158,088 DDX55, LOC105370041, 5 more genes
    nsv7060699inversion1nstd229human GRCh38 chr12: 123,628,133-123,666,880 , GRCh37.p13 chr12: 124,112,680-124,151,427 EIF2B1, GTF2H3
    nsv6938085copy number variation1nstd229human GRCh38 chr12: 123,522,514-123,670,678 , GRCh37.p13 chr12: 124,007,061-124,155,225 TMED2, GTF2H3, 8 more genes
    nsv6934866copy number variation1nstd229human GRCh38 chr12: 119,918,701-123,974,100 , GRCh37.p13 chr12: 120,356,505-124,458,647 RNU6-1088P, LOC105370042, 130 more genes
    nsv6934455copy number variation1nstd229human GRCh38 chr12: 123,232,501-123,974,100 , GRCh37.p13 chr12: 123,717,048-124,458,647 MPHOSPH9, MIR8072, 27 more genes
    nsv6932946copy number variation1nstd229human GRCh38 chr12: 123,628,459-123,712,468 , GRCh37.p13 chr12: 124,113,006-124,197,015 EIF2B1, GTF2H3, 3 more genes
    nsv6932939copy number variation1nstd229human GRCh38 chr12: 123,655,140-123,703,741 , GRCh37.p13 chr12: 124,139,687-124,188,288 GTF2H3, TCTN2
    nsv6932666copy number variation1nstd229human GRCh38 chr12: 123,581,187-123,642,512 , GRCh37.p13 chr12: 124,065,734-124,127,059 DDX55, EIF2B1, 5 more genes
    nsv6926595copy number variation1nstd229human GRCh38 chr12: 123,643,233-123,660,504 , GRCh37.p13 chr12: 124,127,780-124,145,051 GTF2H3
    nsv6923985copy number variation1nstd229human GRCh38 chr12: 123,155,001-123,808,300 , GRCh37.p13 chr12: 123,639,548-124,292,847 TMED2-DT, EIF2B1, 24 more genes
    nsv6921930copy number variation1nstd229human GRCh38 chr12: 123,640,432-123,644,520 , GRCh37.p13 chr12: 124,124,979-124,129,067 GTF2H3
    nsv6921065copy number variation1nstd229human GRCh38 chr12: 123,662,850-123,667,076 , GRCh37.p13 chr12: 124,147,397-124,151,623 GTF2H3
    nsv6918243copy number variation1nstd229human GRCh38 chr12: 123,555,501-123,807,800 , GRCh37.p13 chr12: 124,040,048-124,292,347 RPL27P12, SNORA9B, 11 more genes
    nsv6621551copy number variation1nstd224human GRCh37 chr12: 124,115,018-124,194,438 , GRCh38.p12 chr12: 123,630,471-123,709,891 EIF2B1, TCTN2, 1 more genes
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