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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077157inversion1nstd229human GRCh38 chr8: 144,870,554-144,877,271 , GRCh37.p13 chr8: 146,095,939-146,102,656 ZNF250
    nsv7076836inversion1nstd229human GRCh38 chr8: 144,824,592-144,907,471 , GRCh37.p13 chr8: 146,049,977-146,132,856 ZNF7, ZNF250, 2 more genes
    nsv7064993inversion1nstd229human GRCh38 chr8: 144,871,017-144,898,116 , GRCh37.p13 chr8: 146,096,402-146,123,501 ZNF250
    nsv6875656copy number variation1nstd229human GRCh38 chr8: 144,844,535-144,907,912 , GRCh37.p13 chr8: 146,069,920-146,133,297 ZNF250, COMMD5, 1 more genes
    nsv6873736copy number variation1nstd229human GRCh38 chr8: 144,766,717-145,025,810 , GRCh37.p13 chr8: 145,992,102-146,251,196 RPL8, LOC105375805, 12 more genes
    nsv6873298copy number variation1nstd229human GRCh38 chr8: 144,875,516-144,877,263 , GRCh37.p13 chr8: 146,100,901-146,102,648 ZNF250
    nsv6872694copy number variation1nstd229human GRCh38 chr8: 144,890,537-145,058,091 , GRCh37.p13 chr8: 146,115,922-146,283,477 ZNF252P-AS1, C8orf33, 5 more genes
    nsv6869325copy number variation1nstd229human GRCh38 chr8: 144,896,169-144,907,470 , GRCh37.p13 chr8: 146,121,554-146,132,855 ZNF250
    nsv6866054copy number variation1nstd229human GRCh38 chr8: 144,875,861-144,890,879 , GRCh37.p13 chr8: 146,101,246-146,116,264 ZNF250
    nsv6865630copy number variation1nstd229human GRCh38 chr8: 144,800,681-144,905,297 , GRCh37.p13 chr8: 146,026,066-146,130,682 ZNF250, COMMD5, 3 more genes
    nsv6864556copy number variation1nstd229human GRCh38 chr8: 144,855,742-144,907,103 , GRCh37.p13 chr8: 146,081,127-146,132,488 ZNF250
    nsv6864375copy number variation1nstd229human GRCh38 chr8: 144,880,862-144,880,949 , GRCh37.p13 chr8: 146,106,247-146,106,334 ZNF250
    nsv6864162copy number variation1nstd229human GRCh38 chr8: 144,896,409-144,905,163 , GRCh37.p13 chr8: 146,121,794-146,130,548 ZNF250
    nsv6637599copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,899,733-146,107,871 , GRCh38.p12 chr8: 144,674,348-144,882,486 LOC107986986, LOC100130027, 12 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6632576copy number variation1nstd224human GRCh37 chr8: 146,063,854-146,174,584 , GRCh38.p12 chr8: 144,838,469-144,949,198 ZNF16, ZNF250, 2 more genes
    nsv6563586inversion1nstd223human GRCh38 chr8: 144,885,482-144,886,089 , GRCh37.p13 chr8: 146,110,867-146,111,474 ZNF250
    nsv6558782inversion1nstd223human GRCh38 chr8: 143,001,224-145,028,420 , GRCh37.p13 chr8: 144,082,641-146,253,806 ZFP41, LY6H, 118 more genes
    nsv6429650copy number variation1nstd223human GRCh38 chr8: 144,687,575-144,884,662 , GRCh37.p13 chr8: 145,912,960-146,110,047 MIR6850, ZNF7, 12 more genes
    nsv6427000copy number variation1nstd223human GRCh38 chr8: 144,875,507-144,877,262 , GRCh37.p13 chr8: 146,100,892-146,102,647 ZNF250
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