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Items: 1 to 20 of 236

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 LOC105377327, LOC105377324, 214 more genes
    nsv7050497inversion1nstd229human GRCh38 chr4: 84,984,075-84,993,298 , GRCh37.p13 chr4: 85,905,228-85,914,451 WDFY3-AS2
    nsv7048773inversion1nstd229human GRCh38 chr4: 84,299,895-85,281,334 , GRCh37.p13 chr4: 85,221,048-86,202,487 WDFY3-AS2, CDS1, 8 more genes
    nsv6756256copy number variation1nstd229human GRCh38 chr4: 84,971,826-84,978,486 , GRCh37.p13 chr4: 85,892,979-85,899,639 WDFY3-AS2
    nsv6755120copy number variation1nstd229human GRCh38 chr4: 84,945,506-84,975,025 , GRCh37.p13 chr4: 85,866,659-85,896,178 WDFY3-AS2, WDFY3
    nsv6749303copy number variation1nstd229human GRCh38 chr4: 84,988,508-84,990,369 , GRCh37.p13 chr4: 85,909,661-85,911,522 WDFY3-AS2
    nsv6748280copy number variation1nstd229human GRCh38 chr4: 84,960,601-84,966,600 , GRCh37.p13 chr4: 85,881,754-85,887,753 WDFY3-AS2, WDFY3
    nsv6744392copy number variation1nstd229human GRCh38 chr4: 84,981,201-84,984,200 , GRCh37.p13 chr4: 85,902,354-85,905,353 WDFY3-AS2
    nsv6741958copy number variation1nstd229human GRCh38 chr4: 84,970,543-84,973,548 , GRCh37.p13 chr4: 85,891,696-85,894,701 WDFY3-AS2
    nsv6741586copy number variation1nstd229human GRCh38 chr4: 85,008,101-85,034,200 , GRCh37.p13 chr4: 85,929,254-85,955,353 WDFY3-AS2
    nsv6740374copy number variation1nstd229human GRCh38 chr4: 84,793,845-84,997,269 , GRCh37.p13 chr4: 85,714,998-85,918,422 RNU6-469P, WDFY3-AS2, 1 more genes
    nsv6568263inversion1nstd223human GRCh38 chr4: 84,964,211-84,964,795 , GRCh37.p13 chr4: 85,885,364-85,885,948 WDFY3-AS2, WDFY3
    nsv6567926inversion1nstd223human GRCh38 chr4: 85,001,447-85,001,914 , GRCh37.p13 chr4: 85,922,600-85,923,067 WDFY3-AS2
    nsv6392784copy number variation1nstd223human GRCh38 chr4: 84,977,468-84,977,865 , GRCh37.p13 chr4: 85,898,621-85,899,018 WDFY3-AS2
    nsv6386359copy number variation1nstd223human GRCh38 chr4: 84,962,901-84,965,900 , GRCh37.p13 chr4: 85,884,054-85,887,053 WDFY3-AS2, WDFY3
    nsv6385605copy number variation1nstd223human GRCh38 chr4: 84,971,826-84,978,480 , GRCh37.p13 chr4: 85,892,979-85,899,633 WDFY3-AS2
    nsv6313848copy number variation1nstd102humanPathogenic GRCh37 chr4: 81,054,789-90,667,421 , GRCh38.p12 chr4: 80,133,635-89,746,270 RPL6P13, SNORD144, 136 more genes
    nsv6313510copy number variation1nstd102humanPathogenic GRCh37 chr4: 75,737,340-91,131,156 , GRCh38.p12 chr4: 74,812,130-90,210,005 HIGD1AP13, CXCL11, 240 more genes
    nsv6313484copy number variation1nstd102humanPathogenic GRCh37 chr4: 79,780,152-94,873,225 , GRCh38.p12 chr4: 78,858,998-93,952,074 LOC105377329, LOC107986294, 166 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
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