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Items: 1 to 20 of 221

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5907175copy number variation1nstd209human GRCh38 chr3: 13,311,898-13,315,690 , GRCh37.p13 chr3: 13,353,398-13,357,190 NUP210
    nsv5834914copy number variation1nstd209human GRCh38 chr3: 13,311,919-13,315,699 , GRCh37.p13 chr3: 13,353,419-13,357,199 NUP210
    nsv5623317insertion1nstd207human GRCh38 chr3: 13,377,787-13,377,787 , GRCh37.p13 chr3: 13,419,287-13,419,287 NUP210
    nsv5622358insertion1nstd207human GRCh38 chr3: 13,331,032-13,331,032 , GRCh37.p13 chr3: 13,372,532-13,372,532 NUP210
    nsv5615788insertion1nstd207human GRCh38 chr3: 13,330,458-13,330,458 , GRCh37.p13 chr3: 13,371,958-13,371,958 NUP210
    nsv5568971copy number variation1nstd207human GRCh38 chr3: 13,377,787-13,377,852 , GRCh37.p13 chr3: 13,419,287-13,419,352 NUP210
    nsv5447547copy number variation1nstd206human GRCh38 chr3: 13,419,261-13,419,872 , GRCh37.p13 chr3: 13,460,761-13,461,372 NUP210
    nsv5445095copy number variation1nstd206human GRCh38 chr3: 13,348,910-13,349,050 , GRCh37.p13 chr3: 13,390,410-13,390,550 NUP210
    nsv5351458translocation1nstd200human GRCh38 chr3: 129,333,363-129,333,363 , GRCh38 chr3: 13,349,050-13,349,050 , GRCh37.p13 chr3: 129,052,206-129,052,206 , GRCh37.p13 chr3: 13,390,550-13,390,550 NUP210, MARK2P3
    nsv5341637translocation1nstd200human GRCh37 chr3: 13,390,548-13,390,548 , GRCh37 chr3: 129,052,206-129,052,206 , GRCh38.p12 chr3: 13,349,048-13,349,048 , GRCh38.p12 chr3: 129,333,363-129,333,363 MARK2P3, NUP210
    nsv5308286copy number variation1nstd204human GRCh38.p13 chr3: 13,336,176-13,344,725 , GRCh37.p13 chr3: 13,377,676-13,386,225 NUP210
    nsv5209237copy number variation1nstd204human GRCh38.p13 chr3: 13,342,702-13,344,101 , GRCh37.p13 chr3: 13,384,202-13,385,601 NUP210
    nsv5202857copy number variation1nstd204human GRCh38.p13 chr3: 13,336,152-13,344,990 , GRCh37.p13 chr3: 13,377,652-13,386,490 NUP210
    nsv5078733mobile element insertion1nstd203human GRCh38 chr3: 13,349,050-13,349,050 , GRCh37.p13 chr3: 13,390,550-13,390,550 NUP210
    nsv5065407mobile element insertion1nstd203human GRCh38 chr3: 13,349,049-13,349,049 , GRCh37.p13 chr3: 13,390,549-13,390,549 NUP210
    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
    nsv4924195copy number variation1nstd200human GRCh38 chr3: 13,327,171-13,332,461 , GRCh37.p13 chr3: 13,368,671-13,373,961 NUP210
    nsv4917872copy number variation1nstd200human GRCh38 chr3: 13,345,501-13,346,552 , GRCh37.p13 chr3: 13,387,001-13,388,052 NUP210
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
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