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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7063163inversion1nstd229human GRCh38 chr8: 59,556,849-59,569,860 , GRCh37.p13 chr8: 60,469,408-60,482,419 NUDT15P1
    nsv7058858inversion1nstd229human GRCh38 chr8: 59,557,162-59,563,628 , GRCh37.p13 chr8: 60,469,721-60,476,187 NUDT15P1
    nsv6855995copy number variation1nstd229human GRCh38 chr8: 59,489,151-59,557,278 , GRCh37.p13 chr8: 60,401,710-60,469,837 NUDT15P1
    nsv6853933copy number variation1nstd229human GRCh38 chr8: 59,153,072-60,491,960 , GRCh37.p13 chr8: 60,065,631-61,404,519 SLC2A13P1, LOC105375859, 10 more genes
    nsv6841239copy number variation1nstd229human GRCh38 chr8: 58,126,751-59,593,730 , GRCh37.p13 chr8: 59,039,310-60,506,289 RNA5SP267, LOC105375860, 15 more genes
    nsv6136687copy number variation1nstd213human GRCh37 chr8: 60,060,000-61,250,001 , GRCh38.p12 chr8: 59,147,441-60,337,442 CA8, NUDT15P1, 8 more genes
    nsv6136681copy number variation1nstd213human GRCh37 chr8: 46,860,000-86,550,001 , GRCh38.p12 chr8: 45,948,378-85,637,772 CEBPD, EYA1, 519 more genes
    nsv6136061copy number variation1nstd213human GRCh37 chr8: 54,780,000-63,060,001 , GRCh38.p12 chr8: 53,867,440-62,147,442 RAB2A, SDCBP, 117 more genes
    nsv5705424mobile element insertion1nstd211human GRCh38 chr8: 59,555,236-59,555,236 , GRCh37.p13 chr8: 60,467,795-60,467,795 NUDT15P1
    nsv5396875mobile element insertion1nstd206human GRCh38 chr8: 59,555,236-59,555,287 , GRCh37.p13 chr8: 60,467,795-60,467,846 NUDT15P1
    nsv5102695mobile element insertion1nstd203human GRCh38 chr8: 59,556,656-59,556,672 , GRCh37.p13 chr8: 60,469,215-60,469,231 NUDT15P1
    nsv4716589copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 60,026,663-63,779,735 , GRCh38.p12 chr8: 59,114,104-62,867,176 ASPH, CA8, 36 more genes
    nsv4456871copy number variation1nstd102humanPathogenic GRCh37 chr8: 39,555,657-64,049,089 , GRCh38.p12 chr8: 39,698,138-63,136,530 CRIPTOP5, TRIM60P15, 297 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4318272inversion1nstd166human GRCh37.p13 chr8: 51,271,211-76,167,888 , GRCh38.p12 chr8: 50,358,651-75,255,653 , ASPH, 341 more genes
    nsv3955337copy number variation1nstd168human GRCh38 chr8: 59,535,267-59,557,721 , GRCh37.p13 chr8: 60,447,826-60,470,280 NUDT15P1
    nsv3923517copy number variation1nstd102humanPathogenic NCBI36 chr8: 36,556,779-60,694,111 , GRCh37 chr8: 36,437,621-60,531,557 , GRCh38 chr8: 36,580,103-59,618,998 LOC105379380, TPT1P8, 320 more genes
    nsv3923501copy number variation1nstd102humanPathogenic NCBI36 chr8: 55,896,471-62,221,415 , GRCh38 chr8: 54,821,357-61,146,302 , GRCh37 chr8: 55,733,917-62,058,861 NUDT15P1, LINC01301, 83 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
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