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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5891025copy number variation1nstd209human GRCh38 chr3: 49,693,626-52,462,904 , GRCh37.p13 chr3: 49,731,059-52,496,920 , SEMA3G, 106 more genes
    nsv5890625copy number variation1nstd209human GRCh38 chr3: 52,073,317-52,073,451 , GRCh37.p13 chr3: 52,107,333-52,107,467 POC1A
    nsv5836663copy number variation1nstd209human GRCh38 chr3: 52,111,115-52,112,114 , GRCh37.p13 chr3: 52,145,131-52,146,130 POC1A
    nsv5683783mobile element insertion2nstd211human GRCh38 chr3: 52,135,986-52,135,986 , GRCh37.p13 chr3: 52,170,002-52,170,002 POC1A
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5397191mobile element insertion1nstd206human GRCh38 chr3: 52,135,986-52,136,037 , GRCh37.p13 chr3: 52,170,002-52,170,053 POC1A
    nsv5351765translocation1nstd200human GRCh38 chr3: 52,098,838-52,098,838 , GRCh38 chr3: 52,102,852-52,102,852 , GRCh37.p13 chr3: 52,132,854-52,132,854 , GRCh37.p13 chr3: 52,136,868-52,136,868 POC1A
    nsv5200746copy number variation1nstd204human GRCh38.p13 chr3: 52,056,901-52,406,800 , GRCh37.p13 chr3: 52,090,917-52,440,816 ALAS1, BAP1, 16 more genes
    nsv5184927mobile element insertion1nstd203human GRCh38 chr3: 52,144,317-52,144,317 , GRCh37.p13 chr3: 52,178,333-52,178,333 POC1A
    nsv5076347mobile element insertion1nstd203human GRCh38 chr3: 52,135,970-52,135,986 , GRCh37.p13 chr3: 52,169,986-52,170,002 POC1A
    nsv5070185mobile element insertion1nstd203human GRCh38 chr3: 52,135,986-52,135,986 , GRCh37.p13 chr3: 52,170,002-52,170,002 POC1A
    nsv5064528mobile element insertion1nstd203human GRCh38 chr3: 52,135,969-52,135,986 , GRCh37.p13 chr3: 52,169,985-52,170,002 POC1A
    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
    nsv4911363copy number variation1nstd200human GRCh38 chr3: 52,090,708-52,095,052 , GRCh37.p13 chr3: 52,124,724-52,129,068 POC1A
    nsv4911347copy number variation1nstd200human GRCh38 chr3: 51,769,352-52,724,007 , GRCh37.p13 chr3: 51,803,368-52,758,023 , ACY1, 55 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
    nsv4790711copy number variation1nstd200human GRCh37 chr3: 52,124,724-52,129,068 , GRCh38.p12 chr3: 52,090,708-52,095,052 POC1A
    nsv4790701copy number variation1nstd200human GRCh37 chr3: 51,803,368-52,758,023 , GRCh38.p12 chr3: 51,769,352-52,724,007 , SNORD19B, 55 more genes
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