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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5671625inversion1nstd207human GRCh38 chr8: 7,301,025-12,600,730 , GRCh37.p13 chr8: 7,158,547-12,458,239 , BLK, 188 more genes
    nsv5671585inversion1nstd207human GRCh38 chr8: 7,927,123-8,236,465 , GRCh37.p13 chr8: 7,784,645-8,093,987 , FAM86B3P, 18 more genes
    nsv5426238copy number variation1nstd206human GRCh38 chr8: 8,016,900-8,033,127 , GRCh37.p13 chr8: 7,874,422-7,890,649 FAM90A12, FAM90A24, 1 more genes
    nsv5259970copy number variation1nstd204human GRCh38.p13 chr8: 8,013,901-8,021,400 , GRCh37.p13 chr8: 7,871,423-7,878,922 FAM90A11, FAM90A24
    nsv5259624copy number variation1nstd204human GRCh38.p13 chr8: 8,017,401-8,018,500 , GRCh37.p13 chr8: 7,874,923-7,876,022 FAM90A24, FAM90A11
    nsv5259250copy number variation1nstd204human GRCh38.p13 chr8: 7,986,001-8,021,300 , GRCh37.p13 chr8: 7,843,523-7,878,822 FAM90A11, FAM90A24, 2 more genes
    nsv5258537copy number variation1nstd204human GRCh38.p13 chr8: 8,013,901-8,016,900 , GRCh37.p13 chr8: 7,871,423-7,874,422 FAM90A11
    nsv5256150copy number variation1nstd204human GRCh38.p13 chr8: 7,888,001-8,016,200 , GRCh37.p13 chr8: 7,745,523-7,873,722 HSPD1P2, DEFB4A, 8 more genes
    nsv5255375copy number variation1nstd204human GRCh38.p13 chr8: 8,011,001-8,021,300 , GRCh37.p13 chr8: 7,868,523-7,878,822 FAM90A11, FAM90A24
    nsv5251765copy number variation1nstd204human GRCh38.p13 chr8: 8,010,801-8,016,900 , GRCh37.p13 chr8: 7,868,323-7,874,422 FAM90A11
    nsv5249573copy number variation1nstd204human GRCh38.p13 chr8: 8,011,501-8,013,300 , GRCh37.p13 chr8: 7,869,023-7,870,822 FAM90A11
    nsv5247855copy number variation1nstd204human GRCh38.p13 chr8: 8,016,901-8,019,700 , GRCh37.p13 chr8: 7,874,423-7,877,222 FAM90A11, FAM90A24
    nsv5246352copy number variation1nstd204human GRCh38.p13 chr8: 8,016,901-8,029,600 , GRCh37.p13 chr8: 7,874,423-7,887,122 FAM90A12, FAM90A11, 1 more genes
    nsv5240589copy number variation1nstd204human GRCh38.p13 chr8: 7,886,901-8,016,100 , GRCh37.p13 chr8: 7,744,423-7,873,622 DEFB108A, LOC392187, 8 more genes
    nsv5240482copy number variation1nstd204human GRCh38.p13 chr8: 8,016,901-8,022,500 , GRCh37.p13 chr8: 7,874,423-7,880,022 FAM90A24, FAM90A11
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4730173inversion85nstd198human GRCh38 chr8: 7,052,376-12,760,459 , GRCh37.p13 chr8: 6,909,898-12,617,968 , BLK, 214 more genes
    nsv4685988copy number variation1nstd102humanPathogenic GRCh37 chr8: 161,516-11,516,619 , GRCh38.p12 chr8: 211,516-11,659,110 ZNF705B, RNU6-682P, 232 more genes
    nsv4680983copy number variation1nstd189human GRCh37.p13 chr8: 7,214,612-7,949,490 , GRCh38.p12 chr8: 7,357,090-8,091,968 , DEFB4A, 55 more genes
    nsv4680905copy number variation1nstd189human GRCh37.p13 chr8: 7,024,568-8,072,303 , GRCh38.p12 chr8: 7,167,046-8,214,781 , DEFB4A, 78 more genes
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