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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053224inversion1nstd229human GRCh38 chr6: 52,383,867-53,956,565 , GRCh37.p13 chr6: 52,248,665-53,821,363 RPA3P2, RN7SKP256, 43 more genes
    nsv7039225inversion1nstd229human GRCh38 chr6: 52,383,865-53,974,829 , GRCh37.p13 chr6: 52,248,663-53,839,627 MIR5685, GSTA8P, 43 more genes
    nsv6786317copy number variation1nstd229human GRCh38 chr6: 52,977,080-52,981,878 , GRCh37.p13 chr6: 52,841,878-52,846,676 GSTA4
    nsv6785006copy number variation1nstd229human GRCh38 chr6: 52,995,787-52,995,968 , GRCh37.p13 chr6: 52,860,585-52,860,766 RN7SK, GSTA4
    nsv6783785copy number variation1nstd229human GRCh38 chr6: 52,975,658-52,976,993 , GRCh37.p13 chr6: 52,840,456-52,841,791 GSTA4
    nsv6781368copy number variation1nstd229human GRCh38 chr6: 52,984,703-52,997,752 , GRCh37.p13 chr6: 52,849,501-52,862,550 GSTA4, RN7SK
    nsv6780545copy number variation1nstd229human GRCh38 chr6: 52,993,001-52,995,400 , GRCh37.p13 chr6: 52,857,799-52,860,198 GSTA4, RN7SK
    nsv6634799copy number variation1nstd227human GRCh38.p12 chr6: 52,799,015-53,098,273 , GRCh37 chr6: 52,663,813-52,963,071 GSTA1, GSTA3, 11 more genes
    nsv6631423copy number variation1nstd224human GRCh37 chr6: 52,648,106-52,881,818 , GRCh38.p12 chr6: 52,783,308-53,017,020 GSTA4, LOC105375091, 9 more genes
    nsv6563073inversion1nstd223human GRCh38 chr6: 52,107,269-56,893,586 , GRCh37.p13 chr6: 51,972,067-56,758,384 GSTA1, LOC730101, 79 more genes
    nsv6408516copy number variation1nstd223human GRCh38 chr6: 52,977,078-52,981,875 , GRCh37.p13 chr6: 52,841,876-52,846,673 GSTA4
    nsv6400533copy number variation1nstd223human GRCh38 chr6: 52,995,787-52,995,968 , GRCh37.p13 chr6: 52,860,585-52,860,766 RN7SK, GSTA4
    nsv6396059copy number variation1nstd223human GRCh38 chr6: 52,849,393-52,994,904 , GRCh37.p13 chr6: 52,714,191-52,859,702 LOC105375091, GSTA11P, 5 more genes
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 ACTG1P9, CRISP1, 245 more genes
    nsv6177656copy number variation1nstd214human GRCh38 chr6: 52,989,947-52,990,017 , GRCh37.p13 chr6: 52,854,745-52,854,815 GSTA4
    nsv6074087insertion1nstd212human GRCh38 chr6: 52,995,818-52,995,818 , GRCh37.p13 chr6: 52,860,616-52,860,616 RN7SK, GSTA4
    nsv5898045copy number variation1nstd209human GRCh38 chr6: 52,989,947-52,990,017 , GRCh37.p13 chr6: 52,854,745-52,854,815 GSTA4
    nsv5893416copy number variation1nstd209human GRCh38 chr6: 52,994,562-52,995,774 , GRCh37.p13 chr6: 52,859,360-52,860,572 GSTA4, RN7SK
    nsv5891851copy number variation1nstd209human GRCh38 chr6: 52,995,787-52,995,967 , GRCh37.p13 chr6: 52,860,585-52,860,765 RN7SK, GSTA4
    nsv5715391mobile element insertion1nstd211human GRCh38 chr6: 52,991,003-52,991,003 , GRCh37.p13 chr6: 52,855,801-52,855,801 GSTA4
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