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Items: 1 to 20 of 111

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7051996inversion1nstd229human GRCh38 chr3: 43,186,996-45,060,828 , GRCh37.p13 chr3: 43,228,488-45,102,320 ABHD5, CLEC3B, 44 more genes
    nsv7038909inversion1nstd229human GRCh38 chr3: 40,520,096-45,093,302 , GRCh37.p13 chr3: 40,561,587-45,134,794 ABHD5, ZKSCAN7, 97 more genes
    nsv6717697copy number variation1nstd229human GRCh38 chr3: 44,537,739-44,740,816 , GRCh37.p13 chr3: 44,579,231-44,782,308 ZNF660, LOC105377056, 11 more genes
    nsv6717338copy number variation1nstd229human GRCh38 chr3: 44,630,649-44,634,585 , GRCh37.p13 chr3: 44,672,141-44,676,077 ZNF660-ZNF197, ZNF197, 1 more genes
    nsv6709622copy number variation1nstd229human GRCh38 chr3: 44,612,122-44,637,298 , GRCh37.p13 chr3: 44,653,614-44,678,790 ZNF660-ZNF197, ZNF197, 2 more genes
    nsv6706862copy number variation1nstd229human GRCh38 chr3: 43,255,168-44,930,739 , GRCh37.p13 chr3: 43,296,660-44,972,231 LOC101928529, ANO10, 40 more genes
    nsv6134813copy number variation1nstd213human GRCh37 chr3: 44,650,000-45,860,001 , GRCh38.p12 chr3: 44,608,508-45,818,509 TGM4, CLEC3B, 35 more genes
    nsv5442365copy number variation1nstd206human GRCh38 chr3: 44,629,776-44,629,963 , GRCh37.p13 chr3: 44,671,268-44,671,455 ZNF197, ZKSCAN7-AS1, 1 more genes
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4674744copy number variation1nstd102humanUncertain significance GRCh37 chr3: 44,444,902-45,413,927 , GRCh38.p12 chr3: 44,403,410-45,372,435 RPL12P44, TMEM42, 37 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4560339mobile element insertion1nstd166human GRCh37.p13 chr3: 44,666,071-44,666,071 , GRCh38.p12 chr3: 44,624,579-44,624,579 , GRCh38.p12 chr3|NW_009646197.1: 149,933-149,933 ZNF197, ZNF197-AS1, 2 more genes
    nsv4471646mobile element insertion1nstd166human GRCh37.p13 chr3: 44,687,378-44,687,378 , GRCh38.p12 chr3: 44,645,886-44,645,886 , GRCh38.p12 chr3|NW_009646197.1: 171,240-171,240 ZNF197, ZNF660-ZNF197, 1 more genes
    nsv4079716copy number variation1nstd166human GRCh37.p13 chr3: 44,663,029-44,665,149 , GRCh38.p12 chr3: 44,621,537-44,623,657 , GRCh38.p12 chr3|NW_009646197.1: 146,891-149,011 ZNF197, ZKSCAN7-AS1, 2 more genes
    nsv3967356copy number variation1nstd168human GRCh38 chr3: 44,583,269-44,626,657 , GRCh37.p13 chr3: 44,624,761-44,668,149 ZNF197, ZKSCAN7, 4 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
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