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Items: 1 to 20 of 105

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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
    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
    nsv6699089copy number variation1nstd229human GRCh38 chr3: 44,716,432-44,727,295 , GRCh37.p13 chr3: 44,757,924-44,768,787 ZNF502, LOC105377056
    nsv6362770copy number variation1nstd223human GRCh38 chr3: 44,694,463-44,818,351 , GRCh37.p13 chr3: 44,735,955-44,859,843 KIF15, KIAA1143, 4 more genes
    nsv6276014insertion1nstd214human GRCh38 chr3: 44,722,641-44,722,641 , GRCh37.p13 chr3: 44,764,133-44,764,133 ZNF502, LOC105377056
    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
    nsv5891571copy number variation1nstd209human GRCh38 chr3: 44,722,641-44,722,731 , GRCh37.p13 chr3: 44,764,133-44,764,223 LOC105377056, ZNF502
    nsv5436015copy number variation1nstd206human GRCh38 chr3: 44,722,641-44,722,732 , GRCh37.p13 chr3: 44,764,133-44,764,224 LOC105377056, ZNF502
    nsv5201747copy number variation1nstd204human GRCh38.p13 chr3: 44,718,801-44,724,500 , GRCh37.p13 chr3: 44,760,293-44,765,992 LOC105377056, ZNF502
    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
    nsv4645108copy number variation1nstd186human GRCh37 chr3: 44,764,133-44,764,224 , GRCh38.p12 chr3: 44,722,641-44,722,732 , GRCh38.p12 chr3|NW_009646197.1: 247,991-248,082 ZNF502, LOC105377056
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4073691copy number variation1nstd166human GRCh37.p13 chr3: 44,764,133-44,764,224 , GRCh38.p12 chr3: 44,722,641-44,722,732 , GRCh38.p12 chr3|NW_009646197.1: 247,991-248,082 LOC105377056, ZNF502
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
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