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Items: 1 to 20 of 405

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140410copy number variation1nstd232human GRCh37.p13 chr8: 54,861,092-54,861,153 , GRCh38.p12 chr8: 53,948,532-53,948,593 RGS20
    nsv7071970inversion1nstd229human GRCh38 chr8: 53,827,836-53,959,393 , GRCh37.p13 chr8: 54,740,396-54,871,953 RGS20, RPS27AP13, 2 more genes
    nsv7067508inversion1nstd229human GRCh38 chr8: 51,755,366-56,976,322 , GRCh37.p13 chr8: 52,667,926-57,888,881 CHCHD2P10, LOC105375850, 81 more genes
    nsv7067053inversion1nstd229human GRCh38 chr8: 53,829,999-53,851,810 , GRCh37.p13 chr8: 54,742,559-54,764,370 ATP6V1H, RGS20
    nsv7064051inversion1nstd229human GRCh38 chr8: 53,370,406-56,357,942 , GRCh37.p13 chr8: 54,282,966-57,270,501 CHCHD2P10, RN7SL798P, 51 more genes
    nsv7063863inversion1nstd229human GRCh38 chr8: 53,905,155-53,912,165 , GRCh37.p13 chr8: 54,817,715-54,824,725 RGS20
    nsv6858015copy number variation1nstd229human GRCh38 chr8: 53,906,101-53,985,400 , GRCh37.p13 chr8: 54,818,661-54,897,960 LOC100131254, TCEA1, 2 more genes
    nsv6857203copy number variation1nstd229human GRCh38 chr8: 53,810,158-53,863,109 , GRCh37.p13 chr8: 54,722,718-54,775,669 RGS20, ATP6V1H
    nsv6856143copy number variation1nstd229human GRCh38 chr8: 53,944,257-53,999,017 , GRCh37.p13 chr8: 54,856,817-54,911,577 RGS20, TCEA1, 1 more genes
    nsv6855666copy number variation1nstd229human GRCh38 chr8: 53,851,208-54,150,027 , GRCh37.p13 chr8: 54,763,768-55,062,587 RGS20, LOC105375839, 7 more genes
    nsv6855204copy number variation1nstd229human GRCh38 chr8: 53,905,593-53,910,324 , GRCh37.p13 chr8: 54,818,153-54,822,884 RGS20
    nsv6854773copy number variation1nstd229human GRCh38 chr8: 53,894,234-53,899,230 , GRCh37.p13 chr8: 54,806,794-54,811,790 RGS20
    nsv6848438copy number variation1nstd229human GRCh38 chr8: 53,740,801-54,219,926 , GRCh37.p13 chr8: 54,653,361-55,132,486 ATP6V1H, TCEA1, 10 more genes
    nsv6848173copy number variation1nstd229human GRCh38 chr8: 53,848,948-54,247,340 , GRCh37.p13 chr8: 54,761,508-55,159,900 CHCHD2P10, RNU6-1331P, 9 more genes
    nsv6847034copy number variation1nstd229human GRCh38 chr8: 53,894,201-53,895,914 , GRCh37.p13 chr8: 54,806,761-54,808,474 RGS20
    nsv6845474copy number variation1nstd229human GRCh38 chr8: 53,943,300-53,952,284 , GRCh37.p13 chr8: 54,855,860-54,864,844 RGS20
    nsv6844481copy number variation1nstd229human GRCh38 chr8: 53,955,691-53,956,396 , GRCh37.p13 chr8: 54,868,251-54,868,956 RGS20
    nsv6842900copy number variation1nstd229human GRCh38 chr8: 53,936,376-53,992,100 , GRCh37.p13 chr8: 54,848,936-54,904,660 RGS20, LOC100131254, 1 more genes
    nsv6840986copy number variation1nstd229human GRCh38 chr8: 53,917,215-53,919,657 , GRCh37.p13 chr8: 54,829,775-54,832,217 RGS20
    nsv6840860copy number variation1nstd229human GRCh38 chr8: 53,903,806-53,907,391 , GRCh37.p13 chr8: 54,816,366-54,819,951 RGS20
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