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Items: 1 to 20 of 582

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7137114copy number variation1nstd102humanPathogenic GRCh37 chr15: 98,996,113-101,211,899 , GRCh38.p12 chr15: 98,452,884-100,671,694 PGPEP1L, LOC105371017, 36 more genes
    nsv7098892copy number variation1nstd102humanPathogenic GRCh37 chr15: 84,228,005-102,264,590 , GRCh38.p12 chr15: 83,559,253-101,724,387 CIB1, RPS12P26, 326 more genes
    nsv7074837inversion1nstd229human GRCh38 chr15: 98,618,777-101,109,346 , GRCh37.p13 chr15: 99,162,006-101,649,551 LOC440313, PRKXP1, 42 more genes
    nsv7072627inversion1nstd229human GRCh38 chr15: 99,244,644-99,244,689 , GRCh37.p13 chr15: 99,784,849-99,784,894 TTC23
    nsv7065444inversion1nstd229human GRCh38 chr15: 99,248,723-99,248,783 , GRCh37.p13 chr15: 99,788,928-99,788,988 TTC23
    nsv7065226inversion1nstd229human GRCh38 chr15: 98,338,625-100,843,802 , GRCh37.p13 chr15: 98,881,854-101,384,007 LOC102723335, LUNAR1, 39 more genes
    nsv7064824inversion1nstd229human GRCh38 chr15: 98,981,210-99,387,289 , GRCh37.p13 chr15: 99,524,439-99,927,494 SYNM-AS1, TTC23, 6 more genes
    nsv7063694inversion1nstd229human GRCh38 chr15: 98,738,473-100,284,229 , GRCh37.p13 chr15: 99,281,702-100,824,434 MIR4714, PGPEP1L, 22 more genes
    nsv7058435inversion1nstd229human GRCh38 chr15: 99,189,235-99,257,521 , GRCh37.p13 chr15: 99,729,440-99,797,726 HSP90B2P, TTC23, 1 more genes
    nsv6977630copy number variation1nstd229human GRCh38 chr15: 99,234,075-99,244,822 , GRCh37.p13 chr15: 99,774,280-99,785,027 TTC23
    nsv6977420copy number variation1nstd229human GRCh38 chr15: 99,228,901-99,260,000 , GRCh37.p13 chr15: 99,769,106-99,800,205 HSP90B2P, LRRC28, 1 more genes
    nsv6977137copy number variation1nstd229human GRCh38 chr15: 98,919,969-99,497,854 , GRCh37.p13 chr15: 99,463,198-100,038,059 SYNM, LINC02244, 11 more genes
    nsv6976861copy number variation1nstd229human GRCh38 chr15: 99,138,503-99,141,950 , GRCh37.p13 chr15|NW_003871084.1: 13,891-17,338 , GRCh37.p13 chr15: 99,678,708-99,682,155 TTC23
    nsv6976840copy number variation1nstd229human GRCh38 chr15: 99,204,704-99,306,705 , GRCh37.p13 chr15: 99,744,909-99,846,910 HNRNPA1P62, TTC23, 2 more genes
    nsv6975600copy number variation1nstd229human GRCh38 chr15: 98,893,001-99,187,900 , GRCh37.p13 chr15|NW_003871084.1: 1-170,033 , GRCh37.p13 chr15: 99,436,230-99,728,105 IGF1R, PGPEP1L, 4 more genes
    nsv6973783copy number variation1nstd229human GRCh38 chr15: 99,178,265-99,178,490 , GRCh37.p13 chr15: 99,718,470-99,718,695 TTC23
    nsv6973123copy number variation1nstd229human GRCh38 chr15: 99,197,701-99,215,500 , GRCh37.p13 chr15: 99,737,906-99,755,705 TTC23
    nsv6972045copy number variation1nstd229human GRCh38 chr15: 98,854,051-99,246,000 , GRCh37.p13 chr15: 99,397,280-99,786,205 IGF1R, SYNM-AS1, 4 more genes
    nsv6970223copy number variation1nstd229human GRCh38 chr15: 99,186,827-99,193,760 , GRCh37.p13 chr15: 99,727,032-99,733,965 TTC23
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