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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5873281copy number variation1nstd209human GRCh38 chr17: 40,994,922-40,999,343 , GRCh37.p13 chr17: 39,151,174-39,155,595 KRTAP3-2
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5536426insertion1nstd206human GRCh38 chr17: 40,997,430-40,997,430 , GRCh37.p13 chr17: 39,153,682-39,153,682 KRTAP3-2
    nsv5530664copy number variation1nstd206human GRCh38 chr17: 40,995,908-40,997,432 , GRCh37.p13 chr17: 39,152,160-39,153,684 KRTAP3-2
    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
    nsv5358861translocation1nstd200human GRCh38 chr17: 40,997,432-40,997,432 , GRCh38 chr17: 40,995,908-40,995,908 , GRCh37.p13 chr17: 39,152,160-39,152,160 , GRCh37.p13 chr17: 39,153,684-39,153,684 KRTAP3-2
    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
    nsv4631929copy number variation1nstd183human GRCh37 chr17: 39,154,359-39,156,753 , GRCh38.p12 chr17: 40,998,107-41,000,501 , GRCh38.p12 chr17|NW_003871091.1: 147,502-149,896 KRTAP3-2
    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
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4256505copy number variation1nstd166human GRCh37.p13 chr17: 39,150,000-39,156,000 , GRCh38.p12 chr17|NW_003871091.1: 143,143-149,143 , GRCh38.p12 chr17: 40,993,748-40,999,748 KRTAP3-2, KRTAP3-3
    nsv3918835copy number variation1nstd102humanLikely benign GRCh38 chr17: 40,927,571-41,313,858 , NCBI36 chr17: 36,337,349-36,723,636 , GRCh37 chr17: 39,083,823-39,470,110 KRTAP9-2, KRTAP3-3, 42 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
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