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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5900456copy number variation1nstd209human GRCh38 chr3: 52,444,714-52,444,785 , GRCh37.p13 chr3: 52,478,730-52,478,801 , SEMA3G
    nsv5891462copy number variation1nstd209human GRCh38 chr3: 52,444,464-52,444,706 , GRCh37.p13 chr3: 52,478,480-52,478,722 , SEMA3G
    nsv5891025copy number variation1nstd209human GRCh38 chr3: 49,693,626-52,462,904 , GRCh37.p13 chr3: 49,731,059-52,496,920 , SEMA3G, 106 more genes
    nsv5578434copy number variation1nstd207human GRCh38 chr3: 52,444,714-52,444,785 , GRCh37.p13 chr3: 52,478,730-52,478,801 , SEMA3G
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5437676copy number variation1nstd206human GRCh38 chr3: 52,434,600-52,434,900 , GRCh37.p13 chr3: 52,468,616-52,468,916 SEMA3G
    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
    nsv4911375copy number variation1nstd200human GRCh38 chr3: 52,433,911-52,441,608 , GRCh37.p13 chr3: 52,467,927-52,475,624 , SEMA3G
    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
    nsv4790721copy number variation1nstd200human GRCh37 chr3: 52,467,927-52,475,624 , GRCh38.p12 chr3: 52,433,911-52,441,608 , SEMA3G
    nsv4790701copy number variation1nstd200human GRCh37 chr3: 51,803,368-52,758,023 , GRCh38.p12 chr3: 51,769,352-52,724,007 , SNORD19B, 55 more genes
    nsv4738924copy number variation1nstd199human GRCh37 chr3: 52,478,655-52,478,716 , GRCh38.p12 chr3: 52,444,639-52,444,700 , SEMA3G
    nsv4728314copy number variation1nstd102humanUncertain significance GRCh37 chr3: 51,975,459-52,561,678 , GRCh38.p12 chr3: 51,941,443-52,527,662 ABHD14A-ACY1, POC1A, 32 more genes
    nsv4679783copy number variation1nstd189human GRCh37.p13 chr3: 52,082,781-53,128,685 , GRCh38.p12 chr3: 52,048,765-53,094,669 , ALAS1, 50 more genes
    nsv4673975copy number variation1nstd102humanUncertain significance GRCh37 chr3: 51,247,306-53,069,942 , GRCh38.p12 chr3: 51,209,875-53,035,926 RRP9, LOC100301990, 76 more genes
    nsv4586450copy number variation1nstd183human GRCh37 chr3: 52,473,110-52,474,448 , GRCh38.p12 chr3: 52,439,094-52,440,432 SEMA3G
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
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