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Items: 1 to 20 of 358

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054705inversion1nstd229human GRCh38 chr4: 139,663,990-139,670,112 , GRCh37.p13 chr4: 140,585,144-140,591,266 MGST2
    nsv7046888inversion1nstd229human GRCh38 chr4: 139,666,005-139,669,870 , GRCh37.p13 chr4: 140,587,159-140,591,024 MGST2
    nsv7045068inversion1nstd229human GRCh38 chr4: 138,588,072-141,319,129 , GRCh37.p13 chr4: 139,509,226-142,240,283 RN7SKP253, FTH1P24, 41 more genes
    nsv7044154inversion1nstd229human GRCh38 chr4: 139,663,529-139,667,937 , GRCh37.p13 chr4: 140,584,683-140,589,091 MGST2
    nsv6757367copy number variation1nstd229human GRCh38 chr4: 139,604,745-139,700,684 , GRCh37.p13 chr4: 140,525,899-140,621,838 QKILA, MGST2, 3 more genes
    nsv6757179copy number variation1nstd229human GRCh38 chr4: 139,660,239-139,665,319 , GRCh37.p13 chr4: 140,581,393-140,586,473 MGST2
    nsv6755867copy number variation1nstd229human GRCh38 chr4: 139,667,324-139,671,451 , GRCh37.p13 chr4: 140,588,478-140,592,605 MGST2
    nsv6754227copy number variation1nstd229human GRCh38 chr4: 139,706,378-139,709,310 , GRCh37.p13 chr4: 140,627,532-140,630,464 MGST2
    nsv6749180copy number variation1nstd229human GRCh38 chr4: 139,717,530-139,717,634 , GRCh37.p13 chr4: 140,638,684-140,638,788 MAML3, MGST2
    nsv6740833copy number variation1nstd229human GRCh38 chr4: 139,724,811-139,733,011 , GRCh37.p13 chr4: 140,645,965-140,654,165 MGST2, MAML3
    nsv6629537copy number variation1nstd224human GRCh37 chr4: 140,541,695-140,784,867 , GRCh38.p12 chr4: 139,620,541-139,863,713 MGST2, MAML3, 4 more genes
    nsv6629166copy number variation1nstd224human GRCh37 chr4: 140,292,217-140,614,711 , GRCh38.p12 chr4: 139,371,063-139,693,557 MGST2, NAA15, 9 more genes
    nsv6394691copy number variation1nstd223human GRCh38 chr4: 139,701,760-139,703,595 , GRCh37.p13 chr4: 140,622,914-140,624,749 MGST2
    nsv6390199copy number variation1nstd223human GRCh38 chr4: 139,604,745-139,700,680 , GRCh37.p13 chr4: 140,525,899-140,621,834 H3P16, QKILA, 3 more genes
    nsv6388967copy number variation1nstd223human GRCh38 chr4: 139,751,201-139,848,900 , GRCh37.p13 chr4: 140,672,355-140,770,054 MGST2, RN7SKP253, 1 more genes
    nsv6377756copy number variation1nstd223human GRCh38 chr4: 139,667,318-139,671,444 , GRCh37.p13 chr4: 140,588,472-140,592,598 MGST2
    nsv6375818copy number variation1nstd223human GRCh38 chr4: 139,732,145-139,734,623 , GRCh37.p13 chr4: 140,653,299-140,655,777 MGST2, MAML3
    nsv6313878copy number variation1nstd102humanPathogenic GRCh37 chr4: 104,715,235-145,252,595 , GRCh38.p12 chr4: 103,794,078-144,331,443 LINC00613, GYPA, 448 more genes
    nsv6313656copy number variation1nstd102humanUncertain significance GRCh37 chr4: 136,035,308-144,718,930 , GRCh38.p12 chr4: 135,114,153-143,797,777 RPS2P20, LOC105377444, 87 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
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