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Items: 1 to 20 of 271

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145012copy number variation1nstd232human GRCh37.p13 chr10: 43,706,366-43,706,429 , GRCh38.p12 chr10: 43,210,918-43,210,981 RASGEF1A
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7072163inversion1nstd229human GRCh38 chr10: 43,213,638-43,225,267 , GRCh37.p13 chr10: 43,709,086-43,720,715 RASGEF1A
    nsv7071643inversion1nstd229human GRCh38 chr10: 42,146,783-43,722,055 , GRCh37.p13 chr10: 42,642,231-44,217,503 RNU6ATAC11P, EIF3LP2, 48 more genes
    nsv6897913copy number variation1nstd229human GRCh38 chr10: 43,264,308-43,294,340 , GRCh37.p13 chr10: 43,759,756-43,789,788 RASGEF1A
    nsv6894330copy number variation1nstd229human GRCh38 chr10: 43,244,241-43,244,715 , GRCh37.p13 chr10: 43,739,689-43,740,163 RASGEF1A
    nsv6892568copy number variation1nstd229human GRCh38 chr10: 43,204,201-43,254,500 , GRCh37.p13 chr10: 43,699,649-43,749,948 RASGEF1A, LOC107984225
    nsv6891550copy number variation1nstd229human GRCh38 chr10: 43,229,503-43,235,649 , GRCh37.p13 chr10: 43,724,951-43,731,097 RASGEF1A, LOC107984225
    nsv6891330copy number variation1nstd229human GRCh38 chr10: 43,203,484-43,208,798 , GRCh37.p13 chr10: 43,698,932-43,704,246 RASGEF1A
    nsv6888487copy number variation1nstd229human GRCh38 chr10: 43,266,901-43,281,700 , GRCh37.p13 chr10: 43,762,349-43,777,148 RASGEF1A
    nsv6887551copy number variation1nstd229human GRCh38 chr10: 43,244,701-43,469,100 , GRCh37.p13 chr10: 43,740,149-43,964,548 LOC107984226, RASGEF1A, 8 more genes
    nsv6887474copy number variation1nstd229human GRCh38 chr10: 43,231,839-43,239,999 , GRCh37.p13 chr10: 43,727,287-43,735,447 LOC107984225, RASGEF1A
    nsv6883580copy number variation1nstd229human GRCh38 chr10: 42,792,424-46,796,570 , GRCh37.p13 chr10: 43,287,872-46,224,333 RASSF4, AGAP14P, 107 more genes
    nsv6881963copy number variation1nstd229human GRCh38 chr10: 43,231,416-43,262,906 , GRCh37.p13 chr10: 43,726,864-43,758,354 RASGEF1A, LOC107984225
    nsv6879768copy number variation1nstd229human GRCh38 chr10: 43,255,529-43,255,731 , GRCh37.p13 chr10: 43,750,977-43,751,179 RASGEF1A
    nsv6634789copy number variation1nstd227human GRCh38.p12 chr10: 43,254,621-43,259,092 , GRCh37 chr10: 43,750,069-43,754,540 RASGEF1A
    nsv6620372copy number variation1nstd224human GRCh37 chr10: 43,740,067-43,814,896 , GRCh38.p12 chr10: 43,244,619-43,319,448 RASGEF1A, LOC105378271
    nsv6449860copy number variation1nstd223human GRCh38 chr10: 43,229,503-43,235,644 , GRCh37.p13 chr10: 43,724,951-43,731,092 RASGEF1A, LOC107984225
    nsv6437890copy number variation1nstd223human GRCh38 chr10: 43,244,236-43,244,715 , GRCh37.p13 chr10: 43,739,684-43,740,163 RASGEF1A
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