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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076874inversion1nstd229human GRCh38 chr8: 32,976,814-32,976,864 , GRCh37.p13 chr8: 32,834,332-32,834,382 LOC105379362
    nsv7063389inversion1nstd229human GRCh38 chr8: 32,923,274-32,926,798 , GRCh37.p13 chr8: 32,780,792-32,784,316 LOC105379362
    nsv7059114inversion1nstd229human GRCh38 chr8: 32,998,827-32,999,461 , GRCh37.p13 chr8: 32,856,345-32,856,979 LOC105379362
    nsv6857880copy number variation1nstd229human GRCh38 chr8: 33,028,047-33,037,415 , GRCh37.p13 chr8: 32,885,565-32,894,933 LOC105379362
    nsv6857670copy number variation1nstd229human GRCh38 chr8: 32,923,580-32,929,119 , GRCh37.p13 chr8: 32,781,098-32,786,637 LOC105379362
    nsv6855664copy number variation1nstd229human GRCh38 chr8: 33,039,509-33,039,602 , GRCh37.p13 chr8: 32,897,027-32,897,120 LOC105379362, RANP9
    nsv6855498copy number variation1nstd229human GRCh38 chr8: 32,995,156-32,995,181 , GRCh37.p13 chr8: 32,852,674-32,852,699 LOC105379362
    nsv6853450copy number variation1nstd229human GRCh38 chr8: 32,938,901-32,963,000 , GRCh37.p13 chr8: 32,796,419-32,820,518 LOC105379362
    nsv6851823copy number variation1nstd229human GRCh38 chr8: 32,930,177-32,934,698 , GRCh37.p13 chr8: 32,787,695-32,792,216 LOC105379362
    nsv6850745copy number variation1nstd229human GRCh38 chr8: 32,999,714-33,009,029 , GRCh37.p13 chr8: 32,857,232-32,866,547 LOC105379362
    nsv6850355copy number variation1nstd229human GRCh38 chr8: 32,961,001-32,971,300 , GRCh37.p13 chr8: 32,818,519-32,828,818 LOC105379362
    nsv6848356copy number variation1nstd229human GRCh38 chr8: 32,940,901-32,953,700 , GRCh37.p13 chr8: 32,798,419-32,811,218 LOC105379362
    nsv6848153copy number variation1nstd229human GRCh38 chr8: 33,045,590-33,045,713 , GRCh37.p13 chr8: 32,903,108-32,903,231 LOC105379362
    nsv6847707copy number variation1nstd229human GRCh38 chr8: 33,027,410-33,027,642 , GRCh37.p13 chr8: 32,884,928-32,885,160 LOC105379362
    nsv6847399copy number variation1nstd229human GRCh38 chr8: 32,960,901-32,971,200 , GRCh37.p13 chr8: 32,818,419-32,828,718 LOC105379362
    nsv6847226copy number variation1nstd229human GRCh38 chr8: 32,865,701-33,913,200 , GRCh37.p13 chr8: 32,723,219-33,770,718 DUSP26, LOC105379362, 20 more genes
    nsv6845703copy number variation1nstd229human GRCh38 chr8: 33,010,037-33,023,776 , GRCh37.p13 chr8: 32,867,555-32,881,294 MTND2P32, LOC105379362, 2 more genes
    nsv6845645copy number variation1nstd229human GRCh38 chr8: 32,951,748-32,969,991 , GRCh37.p13 chr8: 32,809,266-32,827,509 LOC105379362
    nsv6840526copy number variation1nstd229human GRCh38 chr8: 32,977,521-32,977,611 , GRCh37.p13 chr8: 32,835,039-32,835,129 LOC105379362
    nsv6840355copy number variation1nstd229human GRCh38 chr8: 32,979,796-32,983,299 , GRCh37.p13 chr8: 32,837,314-32,840,817 LOC105379362
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