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Items: 1 to 20 of 761

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053674inversion1nstd229human GRCh38 chr6: 150,636,278-150,640,873 , GRCh37.p13 chr6: 150,957,414-150,962,009 PLEKHG1
    nsv7052780inversion1nstd229human GRCh38 chr6: 150,724,949-150,725,056 , GRCh37.p13 chr6: 151,046,085-151,046,192 PLEKHG1
    nsv7048301inversion1nstd229human GRCh38 chr6: 150,644,948-150,656,003 , GRCh37.p13 chr6: 150,966,084-150,977,139 PLEKHG1
    nsv7046834inversion1nstd229human GRCh38 chr6: 150,669,571-150,673,861 , GRCh37.p13 chr6: 150,990,707-150,994,997 PLEKHG1
    nsv7044202inversion1nstd229human GRCh38 chr6: 149,991,759-150,641,370 , GRCh37.p13 chr6: 150,312,895-150,962,506 RAET1K, IYD, 10 more genes
    nsv7043894inversion1nstd229human GRCh38 chr6: 150,627,852-150,632,543 , GRCh37.p13 chr6: 150,948,988-150,953,679 PLEKHG1
    nsv7042877inversion1nstd229human GRCh38 chr6: 149,723,719-152,206,487 , GRCh37.p13 chr6: 150,044,855-152,527,622 MTHFD1L, RAET1F, 48 more genes
    nsv7041422inversion1nstd229human GRCh38 chr6: 150,201,394-154,373,035 , GRCh37.p13 chr6: 150,522,530-154,694,169 MTHFD1L, MYCT1, 56 more genes
    nsv7039942inversion1nstd229human GRCh38 chr6: 150,708,803-150,708,847 , GRCh37.p13 chr6: 151,029,939-151,029,983 PLEKHG1
    nsv6816163copy number variation1nstd229human GRCh38 chr6: 150,602,106-150,620,617 , GRCh37.p13 chr6: 150,923,242-150,941,753 PLEKHG1
    nsv6816071copy number variation1nstd229human GRCh38 chr6: 150,842,716-150,845,182 , GRCh37.p13 chr6: 151,163,852-151,166,318 PLEKHG1
    nsv6815891copy number variation1nstd229human GRCh38 chr6: 150,673,230-150,673,339 , GRCh37.p13 chr6: 150,994,366-150,994,475 PLEKHG1
    nsv6814980copy number variation1nstd229human GRCh38 chr6: 150,663,984-150,673,524 , GRCh37.p13 chr6: 150,985,120-150,994,660 PLEKHG1
    nsv6813766copy number variation1nstd229human GRCh38 chr6: 150,790,001-151,067,700 , GRCh37.p13 chr6: 151,111,137-151,388,836 PLEKHG1, RNU6-302P, 3 more genes
    nsv6813557copy number variation1nstd229human GRCh38 chr6: 150,632,201-150,634,700 , GRCh37.p13 chr6: 150,953,337-150,955,836 PLEKHG1
    nsv6812800copy number variation1nstd229human GRCh38 chr6: 150,714,983-150,715,035 , GRCh37.p13 chr6: 151,036,119-151,036,171 PLEKHG1
    nsv6812307copy number variation1nstd229human GRCh38 chr6: 150,708,455-150,708,801 , GRCh37.p13 chr6: 151,029,591-151,029,937 PLEKHG1
    nsv6810127copy number variation1nstd229human GRCh38 chr6: 150,810,497-150,810,537 , GRCh37.p13 chr6: 151,131,633-151,131,673 PLEKHG1
    nsv6810106copy number variation1nstd229human GRCh38 chr6: 150,711,876-150,720,014 , GRCh37.p13 chr6: 151,033,012-151,041,150 PLEKHG1
    nsv6809949copy number variation1nstd229human GRCh38 chr6: 150,601,914-150,609,685 , GRCh37.p13 chr6: 150,923,050-150,930,821 PLEKHG1
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