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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv5906067copy number variation1nstd209human GRCh38 chr4: 22,920,705-27,042,181 , GRCh37.p13 chr4: 22,922,328-27,043,803 , SEPSECS, 49 more genes
    nsv5892449copy number variation1nstd209human GRCh38 chr4: 24,795,986-24,799,359 , GRCh37.p13 chr4: 24,797,608-24,800,981 SOD3
    nsv5839519copy number variation1nstd209human GRCh38 chr4: 24,796,251-24,799,361 , GRCh37.p13 chr4: 24,797,873-24,800,983 SOD3
    nsv5222016copy number variation1nstd204human GRCh38.p13 chr4: 24,795,108-24,797,182 , GRCh37.p13 chr4: 24,796,730-24,798,804 SOD3
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv4921998copy number variation1nstd200human GRCh38 chr4: 24,792,354-24,793,851 , GRCh37.p13 chr4: 24,793,976-24,795,473 SOD3
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4684161copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-49,620,898 , GRCh38.p12 chr4: 49,556-49,618,881 TLR10, WDR1, 669 more genes
    nsv4674448copy number variation1nstd102humanPathogenic GRCh37 chr4: 20,406,475-29,134,345 , GRCh38.p12 chr4: 20,404,852-29,132,723 LOC100288962, ADGRA3, 84 more genes
    nsv4673983copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-27,423,424 , GRCh38.p12 chr4: 68,453-27,421,802 LOC101928306, LINC02261, 439 more genes
    nsv4521885copy number variation1nstd166human GRCh37.p13 chr4: 24,801,850-24,802,127 , GRCh38.p12 chr4: 24,800,228-24,800,505 SOD3
    nsv4347528copy number variation1nstd102humanPathogenic GRCh37 chr4: 12,778,849-27,760,141 , GRCh38.p12 chr4: 12,777,225-27,758,519 MTCO3P44, LINC01097, 148 more genes
    nsv4101075copy number variation1nstd166human GRCh37.p13 chr4: 24,798,169-24,799,911 , GRCh38.p12 chr4: 24,796,547-24,798,289 SOD3
    nsv3923296copy number variation1nstd102humanPathogenic GRCh38 chr4: 72,555-28,066,309 , NCBI36 chr4: 62,447-27,677,029 , GRCh37 chr4: 72,447-28,067,931 OR7E99P, FBXL5, 446 more genes
    nsv3920498copy number variation1nstd102humanPathogenic NCBI36 chr4: 23,472,721-27,296,266 , GRCh38 chr4: 23,862,000-27,685,546 , GRCh37 chr4: 23,863,623-27,687,168 RNU7-126P, RPS29P11, 48 more genes
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