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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097439copy number variation1nstd102humanUncertain significance GRCh37 chr6: 52,869,947-52,906,034 , GRCh38.p12 chr6: 53,005,149-53,041,236 CILK1
    nsv7053224inversion1nstd229human GRCh38 chr6: 52,383,867-53,956,565 , GRCh37.p13 chr6: 52,248,665-53,821,363 RPA3P2, RN7SKP256, 43 more genes
    nsv7053172inversion1nstd229human GRCh38 chr6: 53,017,209-53,021,767 , GRCh37.p13 chr6: 52,882,007-52,886,565 CILK1
    nsv7039225inversion1nstd229human GRCh38 chr6: 52,383,865-53,974,829 , GRCh37.p13 chr6: 52,248,663-53,839,627 MIR5685, GSTA8P, 43 more genes
    nsv6795736copy number variation1nstd229human GRCh38 chr6: 53,012,740-53,013,111 , GRCh37.p13 chr6: 52,877,538-52,877,909 CILK1
    nsv6794494copy number variation1nstd229human GRCh38 chr6: 53,055,421-53,055,481 , GRCh37.p13 chr6: 52,920,219-52,920,279 CILK1
    nsv6794151copy number variation1nstd229human GRCh38 chr6: 53,037,891-53,043,892 , GRCh37.p13 chr6: 52,902,689-52,908,690 CILK1
    nsv6781047copy number variation1nstd229human GRCh38 chr6: 53,019,721-53,031,922 , GRCh37.p13 chr6: 52,884,519-52,896,720 CILK1
    nsv6780364copy number variation1nstd229human GRCh38 chr6: 53,021,655-53,026,279 , GRCh37.p13 chr6: 52,886,453-52,891,077 CILK1
    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
    nsv6399166copy number variation1nstd223human GRCh38 chr6: 53,035,839-53,037,588 , GRCh37.p13 chr6: 52,900,637-52,902,386 CILK1
    nsv6396651copy number variation1nstd223human GRCh38 chr6: 53,059,001-53,069,400 , GRCh37.p13 chr6: 52,923,799-52,934,198 FBXO9, CILK1
    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
    nsv5725473mobile element insertion1nstd211human GRCh38 chr6: 53,016,776-53,016,776 , GRCh37.p13 chr6: 52,881,574-52,881,574 CILK1
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5554031mobile element insertion1nstd206human GRCh38 chr6: 53,016,776-53,016,827 , GRCh37.p13 chr6: 52,881,574-52,881,625 CILK1
    nsv5470726copy number variation1nstd206human GRCh38 chr6: 53,044,656-53,044,793 , GRCh37.p13 chr6: 52,909,454-52,909,591 CILK1
    nsv5381452copy number variation1nstd102humanUncertain significance GRCh37 chr6: 51,930,764-52,906,034 , GRCh38.p12 chr6: 52,065,966-53,041,236 GSTA4, LOC730101, 30 more genes
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