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Items: 1 to 20 of 91

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968065inversion1nstd209human GRCh38 chr3: 14,742,874-15,551,121 , GRCh37.p13 chr3: 14,784,381-15,592,628 , NR2C2, 21 more genes
    nsv5444573copy number variation1nstd206human GRCh38 chr3: 14,948,103-14,948,171 , GRCh37.p13 chr3: 14,989,610-14,989,678 FGD5-AS1, NR2C2
    nsv5434461copy number variation1nstd206human GRCh38 chr3: 14,912,780-14,996,678 , GRCh37.p13 chr3: 14,954,287-15,038,185 LOC105376963, NR2C2, 2 more genes
    nsv5351465translocation1nstd200human GRCh38 chr3: 14,948,103-14,948,103 , GRCh38 chr3: 14,948,171-14,948,171 , GRCh37.p13 chr3: 14,989,610-14,989,610 , GRCh37.p13 chr3: 14,989,678-14,989,678 FGD5-AS1, NR2C2
    nsv5344154translocation1nstd200human GRCh37 chr3: 14,989,610-14,989,610 , GRCh37 chr3: 14,989,678-14,989,678 , GRCh38.p12 chr3: 14,948,171-14,948,171 , GRCh38.p12 chr3: 14,948,103-14,948,103 NR2C2, FGD5-AS1
    nsv5304849copy number variation1nstd204human GRCh37.p13 chr3: 14,989,587-14,989,702 , GRCh38.p13 chr3: 14,948,080-14,948,195 NR2C2, FGD5-AS1
    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
    nsv4924205copy number variation1nstd200human GRCh38 chr3: 14,931,356-14,944,901 , GRCh37.p13 chr3: 14,972,863-14,986,408 FGD5, FGD5-AS1
    nsv4917928copy number variation1nstd200human GRCh38 chr3: 14,939,715-14,946,581 , GRCh37.p13 chr3: 14,981,222-14,988,088 FGD5-AS1, NR2C2
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4793861copy number variation1nstd200human GRCh37 chr3: 14,954,284-15,038,187 , GRCh38.p12 chr3: 14,912,777-14,996,680 FGD5, NR2C2, 2 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
    nsv4089985copy number variation1nstd166human GRCh37.p13 chr3: 14,987,000-14,992,000 , GRCh38.p12 chr3: 14,945,493-14,950,493 NR2C2, FGD5-AS1
    nsv4084563copy number variation1nstd166human GRCh37.p13 chr3: 14,954,287-15,038,185 , GRCh38.p12 chr3: 14,912,780-14,996,678 NR2C2, FGD5-AS1, 2 more genes
    nsv4075477copy number variation1nstd166human GRCh37.p13 chr3: 14,982,000-14,995,000 , GRCh38.p12 chr3: 14,940,493-14,953,493 FGD5-AS1, NR2C2
    nsv3923656copy number variation1nstd102humanPathogenic GRCh38 chr3: 11,463,328-38,919,543 , NCBI36 chr3: 11,479,802-38,936,038 , GRCh37 chr3: 11,504,802-38,961,034 RN7SL4P, TOP2B, 348 more genes
    nsv3919322copy number variation1nstd102humanPathogenic GRCh38 chr3: 14,360,747-21,656,134 , GRCh37 chr3: 14,402,247-21,697,626 , NCBI36 chr3: 14,377,251-21,672,630 LOC105376988, SLC6A6, 89 more genes
    nsv3907461copy number variation1nstd102humanPathogenic GRCh38 chr3: 63,843-19,510,600 , GRCh37 chr3: 105,526-19,552,092 , NCBI36 chr3: 80,526-19,527,096 TAMM41, CYCSP11, 267 more genes
    nsv3905127copy number variation1nstd102humanPathogenic GRCh37 chr3: 94,991-41,423,012 , NCBI36 chr3: 69,991-41,398,016 , GRCh38 chr3: 53,308-41,381,521 LINC02022, RPL23AP43, 540 more genes
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