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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5904731copy number variation1nstd209human GRCh38 chr2: 144,497,832-144,497,881 , GRCh37.p13 chr2: 145,255,399-145,255,448 ZEB2
    nsv5673372copy number variation1nstd102humanPathogenic GRCh37 chr2: 145,147,018-145,753,167 , GRCh38.p12 chr2: 144,389,451-144,995,600 ZEB2, TEX41, 6 more genes
    nsv5618669insertion1nstd207human GRCh38 chr2: 144,497,981-144,497,981 , GRCh37.p13 chr2: 145,255,548-145,255,548 ZEB2
    nsv5582427copy number variation1nstd207human GRCh38 chr2: 144,497,832-144,497,881 , GRCh37.p13 chr2: 145,255,399-145,255,448 ZEB2
    nsv5564968copy number variation1nstd207human GRCh38 chr2: 144,497,860-144,497,963 , GRCh37.p13 chr2: 145,255,427-145,255,530 ZEB2
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5453195copy number variation1nstd206human GRCh38 chr2: 144,512,971-144,513,063 , GRCh37.p13 chr2: 145,270,538-145,270,630 ZEB2
    nsv5451902copy number variation1nstd206human GRCh38 chr2: 144,379,995-144,546,290 , GRCh37.p13 chr2: 145,137,562-145,303,857 LINC01412, ZEB2, 2 more genes
    nsv5450895copy number variation1nstd206human GRCh38 chr2: 141,459,078-156,842,302 , GRCh37.p13 chr2: 142,216,647-157,698,814 , LOC105373696, 163 more genes
    nsv5445374copy number variation1nstd206human GRCh38 chr2: 144,516,893-144,517,025 , GRCh37.p13 chr2: 145,274,460-145,274,592 ZEB2
    nsv5437048copy number variation1nstd206human GRCh38 chr2: 144,451,402-144,452,202 , GRCh37.p13 chr2: 145,208,969-145,209,769 ZEB2
    nsv5381338copy number variation1nstd102humanPathogenic GRCh37 chr2: 136,473,383-152,727,396 , GRCh38.p12 chr2: 135,715,813-151,870,882 YY1P2, SPOPL, 156 more genes
    nsv5381162copy number variation1nstd102humanUncertain significance GRCh37 chr2: 145,182,343-145,182,454 , GRCh38.p12 chr2: 144,424,776-144,424,887 ZEB2
    nsv5350837translocation1nstd200human GRCh38 chr2: 144,394,196-144,394,196 , GRCh38 chr2: 144,394,258-144,394,258 , GRCh37.p13 chr2: 145,151,763-145,151,763 , GRCh37.p13 chr2: 145,151,825-145,151,825 ZEB2
    nsv5211795copy number variation1nstd204human GRCh38.p13 chr2: 144,497,801-144,498,300 , GRCh37.p13 chr2: 145,255,368-145,255,867 ZEB2
    nsv5174999mobile element insertion1nstd203human GRCh38 chr2: 144,486,952-144,486,968 , GRCh37.p13 chr2: 145,244,519-145,244,535 ZEB2
    nsv5174232mobile element insertion1nstd203human GRCh38 chr2: 144,486,954-144,486,968 , GRCh37.p13 chr2: 145,244,521-145,244,535 ZEB2
    nsv5171720mobile element insertion1nstd203human GRCh38 chr2: 144,486,951-144,486,968 , GRCh37.p13 chr2: 145,244,518-145,244,535 ZEB2
    nsv5070073mobile element insertion1nstd203human GRCh38 chr2: 144,495,146-144,495,159 , GRCh37.p13 chr2: 145,252,713-145,252,726 ZEB2
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
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