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Items: 1 to 20 of 642

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098929copy number variation1nstd102humanPathogenic GRCh38 chr3: 195,950,438-197,629,463 , GRCh37.p13 chr3: 195,677,309-197,356,334 LINC01063, RNF168, 52 more genes
    nsv7098781copy number variation1nstd102humanUncertain significance GRCh37 chr3: 195,591,052-197,682,644 , GRCh38.p12 chr3: 195,864,181-197,955,773 ZDHHC19, DLG1, 68 more genes
    nsv7055557inversion1nstd229human GRCh38 chr3: 195,655,301-197,630,693 , GRCh37.p13 chr3: 195,382,172-197,357,564 MIR570HG, RN7SL434P, 66 more genes
    nsv7054880inversion1nstd229human GRCh38 chr3: 196,830,404-196,840,092 , GRCh37.p13 chr3: 196,557,275-196,566,963 PAK2
    nsv7053852inversion1nstd229human GRCh38 chr3: 195,653,753-197,300,599 , GRCh37.p13 chr3: 195,380,624-197,027,470 NCBP2-AS1, SMCO1, 59 more genes
    nsv7053446inversion1nstd229human GRCh38 chr3: 195,340,377-197,478,980 , GRCh37.p13 chr3: 195,061,106-197,205,851 CEP19, ACAP2, 73 more genes
    nsv7047164inversion1nstd229human GRCh38 chr3: 196,815,362-197,824,853 , GRCh37.p13 chr3: 196,542,233-197,551,724 DLG1, RUBCN, 24 more genes
    nsv7044295inversion1nstd229human GRCh38 chr3: 195,547,271-197,153,236 , GRCh37.p13 chr3: 195,274,089-196,880,107 SDHAP1, NCBP2AS2, 64 more genes
    nsv7044261inversion1nstd229human GRCh38 chr3: 195,438,610-197,225,061 , GRCh37.p13 chr3: 195,159,339-196,951,932 MUC4, RPL24P6, 67 more genes
    nsv6730809copy number variation1nstd229human GRCh38 chr3: 196,758,586-196,769,851 , GRCh37.p13 chr3: 196,485,457-196,496,722 PAK2
    nsv6730311copy number variation1nstd229human GRCh38 chr3: 196,760,549-196,766,629 , GRCh37.p13 chr3: 196,487,420-196,493,500 PAK2
    nsv6729462copy number variation1nstd229human GRCh38 chr3: 196,710,301-196,811,400 , GRCh37.p13 chr3: 196,437,172-196,538,271 CEP19, RNU6-42P, 3 more genes
    nsv6728950copy number variation1nstd229human GRCh38 chr3: 196,718,134-196,755,055 , GRCh37.p13 chr3: 196,445,005-196,481,926 RNU4-89P, PIGX, 1 more genes
    nsv6728821copy number variation1nstd229human GRCh38 chr3: 196,202,777-196,997,902 , GRCh37.p13 chr3: 195,929,648-196,724,773 DYNLT2B, RN7SL434P, 35 more genes
    nsv6725478copy number variation1nstd229human GRCh38 chr3: 196,207,115-197,269,106 , GRCh37.p13 chr3: 195,933,986-196,995,977 PAK2, LINC01063, 38 more genes
    nsv6725286copy number variation1nstd229human GRCh38 chr3: 196,377,963-196,914,388 , GRCh37.p13 chr3: 196,104,834-196,641,259 RNF168, RNU6-646P, 19 more genes
    nsv6725046copy number variation1nstd229human GRCh38 chr3: 196,766,129-196,768,346 , GRCh37.p13 chr3: 196,493,000-196,495,217 PAK2
    nsv6724012copy number variation1nstd229human GRCh38 chr3: 196,830,574-196,834,653 , GRCh37.p13 chr3: 196,557,445-196,561,524 PAK2
    nsv6723209copy number variation1nstd229human GRCh38 chr3: 196,780,195-196,781,179 , GRCh37.p13 chr3: 196,507,066-196,508,050 PAK2
    nsv6722480copy number variation1nstd229human GRCh38 chr3: 196,819,244-196,837,769 , GRCh37.p13 chr3: 196,546,115-196,564,640 PAK2
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