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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143755insertion1nstd232human GRCh37.p13 chr3: 52,725,091-52,725,091 , GRCh38.p12 chr3: 52,691,075-52,691,075 GNL3, SNORD69, 2 more genes
    nsv7138617insertion1nstd232human GRCh37.p13 chr3: 52,725,646-52,725,646 , GRCh38.p12 chr3: 52,691,630-52,691,630 GNL3, SNORD69, 1 more genes
    nsv7097206copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,109,903-53,164,416 , GRCh38.p12 chr3: 52,075,887-53,130,400 PHF7, SEMA3G, 47 more genes
    nsv7096813copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,018,081-53,845,433 , GRCh38.p12 chr3: 51,984,065-53,811,406 DNAH1, BAP1, 62 more genes
    nsv7041270inversion1nstd229human GRCh38 chr3: 52,619,221-53,173,329 , GRCh37.p13 chr3: 52,653,237-53,185,061 SNORD19, SNORD19C, 23 more genes
    nsv6717956copy number variation1nstd229human GRCh38 chr3: 52,650,204-52,702,405 , GRCh37.p13 chr3: 52,684,220-52,736,421 SNORD19B, GLT8D1, 6 more genes
    nsv6716874copy number variation1nstd229human GRCh38 chr3: 52,619,220-52,838,314 , GRCh37.p13 chr3: 52,653,236-52,872,330 ITIH4-AS1, STIMATE, 18 more genes
    nsv6715600copy number variation1nstd229human GRCh38 chr3: 52,628,201-52,691,600 , GRCh37.p13 chr3: 52,662,217-52,725,616 SNORD19C, SNORD19, 5 more genes
    nsv6715302copy number variation1nstd229human GRCh38 chr3: 52,656,401-52,872,900 , GRCh37.p13 chr3: 52,690,417-52,906,916 SNORD136, GLT8D1, 19 more genes
    nsv6713675copy number variation1nstd229human GRCh38 chr3: 52,547,701-52,692,100 , GRCh37.p13 chr3: 52,581,717-52,726,116 SNORD19B, SNORD136, 7 more genes
    nsv6709799copy number variation1nstd229human GRCh38 chr3: 52,687,401-52,689,500 , GRCh37.p13 chr3: 52,721,417-52,723,516 SNORD136, SNORD19C, 3 more genes
    nsv6369827copy number variation1nstd223human GRCh38 chr3: 52,164,358-54,467,618 , GRCh37.p13 chr3: 52,198,374-54,501,645 SEMA3G, STAB1, 61 more genes
    nsv6134815copy number variation1nstd213human GRCh37 chr3: 52,350,000-53,060,001 , GRCh38.p12 chr3: 52,315,984-53,025,985 ITIH1, ITIH3, 32 more genes
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5442332copy number variation1nstd206human GRCh38 chr3: 52,690,553-52,692,565 , GRCh37.p13 chr3: 52,724,569-52,726,581 GNL3, SNORD69, 3 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
    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
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