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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv7066656inversion1nstd229human GRCh38 chr17: 40,822,205-41,582,529 , GRCh37.p13 chr17: 38,978,457-39,738,781 LOC105371777, KRT10, 69 more genes
    nsv6992218copy number variation1nstd229human GRCh38 chr17: 40,934,745-41,023,836 , GRCh37.p13 chr17: 39,090,997-39,180,088 KRT40, KRTAP3-1, 6 more genes
    nsv6984984copy number variation1nstd229human GRCh38 chr17: 38,377,708-42,855,253 , GRCh37.p13 chr17: 36,701,616-41,007,270 ZNF385C, AOC2, 248 more genes
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6980804copy number variation1nstd229human GRCh38 chr17: 40,949,294-41,074,654 , GRCh37.p13 chr17: 39,105,546-39,230,906 KRTAP3-3, KRTAP3-1, 14 more genes
    nsv6513343copy number variation1nstd223human GRCh38 chr17: 40,991,568-41,003,812 , GRCh37.p13 chr17: 39,147,820-39,160,064 KRTAP3-3, KRTAP3-4P, 1 more genes
    nsv6512300copy number variation1nstd223human GRCh38 chr17: 40,993,401-40,999,800 , GRCh37.p13 chr17: 39,149,653-39,156,052 KRTAP3-2, KRTAP3-3
    nsv6509451copy number variation1nstd223human GRCh38 chr17: 40,934,745-41,023,836 , GRCh37.p13 chr17: 39,090,997-39,180,088 KRT23, KRTAP3-2, 6 more genes
    nsv6133056copy number variation1nstd213human GRCh37 chr17: 36,400,000-39,740,001 , GRCh38.p12 chr17: 38,545,381-41,583,749 CACNB1, CDC6, 176 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5528952copy number variation1nstd206human GRCh38 chr17: 40,993,980-40,999,980 , GRCh37.p13 chr17: 39,150,232-39,156,232 KRTAP3-3, KRTAP3-2
    nsv5521102copy number variation1nstd206human GRCh38 chr17: 40,993,890-40,999,980 , GRCh37.p13 chr17: 39,150,142-39,156,232 KRTAP3-2, KRTAP3-3
    nsv5518631copy number variation1nstd206human GRCh38 chr17: 40,902,081-41,114,453 , GRCh37.p13 chr17: 39,058,333-39,270,705 KRTAP2-3, LOC105371777, 20 more genes
    nsv5285912copy number variation1nstd204human GRCh38.p13 chr17: 40,993,872-40,999,493 , GRCh37.p13 chr17: 39,150,124-39,155,745 KRTAP3-3, KRTAP3-2
    nsv5016354copy number variation1nstd200human GRCh38 chr17: 40,993,889-40,999,787 , GRCh37.p13 chr17: 39,150,141-39,156,039 KRTAP3-3, KRTAP3-2
    nsv4679355copy number variation1nstd189human GRCh37.p13 chr17: 38,659,900-39,414,647 , GRCh38.p12 chr17: 40,503,648-41,258,395 , CCR7, 54 more genes
    nsv4622576copy number variation1nstd183human GRCh37 chr17: 39,150,213-39,155,969 , GRCh38.p12 chr17|NW_003871091.1: 143,356-149,112 , GRCh38.p12 chr17: 40,993,961-40,999,717 KRTAP3-2, KRTAP3-3
    nsv4622332copy number variation1nstd183human GRCh37 chr17: 39,149,741-39,158,377 , GRCh38.p12 chr17|NW_003871091.1: 142,884-151,520 , GRCh38.p12 chr17: 40,993,489-41,002,125 KRTAP3-2, KRTAP3-3
    nsv4419287copy number variation1nstd174human GRCh37 chr17: 39,150,213-39,156,289 , GRCh38.p12 chr17: 40,993,961-41,000,037 , GRCh38.p12 chr17|NW_003871091.1: 143,356-149,432 KRTAP3-2, KRTAP3-3
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