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Items: 1 to 20 of 125

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5687047mobile element insertion1nstd211human GRCh38 chr3: 42,395,620-42,395,620 , GRCh37.p13 chr3: 42,437,112-42,437,112 LYZL4
    nsv5398498mobile element insertion1nstd206human GRCh38 chr3: 42,395,620-42,395,671 , GRCh37.p13 chr3: 42,437,112-42,437,163 LYZL4
    nsv5351702translocation1nstd200human GRCh38 chr3: 42,388,828-42,388,828 , GRCh38 chr3: 42,388,881-42,388,881 , GRCh37.p13 chr3: 42,430,373-42,430,373 , GRCh37.p13 chr3: 42,430,320-42,430,320 LYZL4
    nsv5338810translocation1nstd200human GRCh37 chr3: 42,430,320-42,430,320 , GRCh37 chr3: 42,430,373-42,430,373 , GRCh38.p12 chr3: 42,388,881-42,388,881 , GRCh38.p12 chr3: 42,388,828-42,388,828 LYZL4
    nsv5307519copy number variation1nstd204human GRCh38.p13 chr3: 41,848,598-42,362,902 , GRCh37.p13 chr3: 41,890,090-42,404,394 SALL4P6, ULK4, 11 more genes
    nsv5209269copy number variation1nstd204human GRCh38.p13 chr3: 41,848,601-42,362,900 , GRCh37.p13 chr3: 41,890,093-42,404,392 ATP6V0E1P2, LOC107986077, 11 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
    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
    nsv4728413copy number variation1nstd102humanUncertain significance GRCh37 chr3: 42,008,472-42,610,176 , GRCh38.p12 chr3: 41,966,980-42,568,684 LYZL4, SEC22C, 12 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4470623mobile element insertion1nstd166human GRCh37.p13 chr3: 42,437,098-42,437,098 , GRCh38.p12 chr3: 42,395,606-42,395,606 LYZL4
    nsv4073280copy number variation1nstd166human GRCh37.p13 chr3: 42,314,398-42,502,034 , GRCh38.p12 chr3: 42,272,906-42,460,542 SALL4P6, EIF4BP4, 1 more genes
    nsv3969139insertion1nstd168human GRCh38 chr3: 42,324,157-42,362,286 , GRCh37.p13 chr3: 42,365,649-42,403,778 LYZL4, EIF4BP4
    nsv3914992copy number variation1nstd102humanUncertain significance GRCh37 chr3: 41,921,995-42,591,771 , GRCh38 chr3: 41,880,503-42,550,279 , NCBI36 chr3: 41,896,999-42,566,775 CCK, EIF4BP4, 14 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
    nsv3885169copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,923,595-45,249,923 , GRCh38.p12 chr3: 16,884,818-45,208,431 RNU6-243P, ZNF385D, 382 more genes
    nsv3883164copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 37,028,313-49,929,220 , GRCh38.p12 chr3: 36,986,822-49,891,787 ACAA1, ACVR2B, 344 more genes
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