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Items: 1 to 20 of 198

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959110insertion1nstd209human GRCh38 chr3: 20,165,582-20,165,582 , GRCh37.p13 chr3: 20,207,074-20,207,074 SGO1
    nsv5904559copy number variation1nstd209human GRCh38 chr3: 20,159,412-20,159,492 , GRCh37.p13 chr3: 20,200,904-20,200,984 SGO1
    nsv5892001copy number variation1nstd209human GRCh38 chr3: 20,054,861-20,362,981 , GRCh37.p13 chr3: 20,096,353-20,404,473 , KAT2B, 6 more genes
    nsv5581378copy number variation1nstd207human GRCh38 chr3: 20,159,412-20,159,492 , GRCh37.p13 chr3: 20,200,904-20,200,984 SGO1
    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
    nsv4746713copy number variation1nstd199human GRCh37 chr3: 20,200,920-20,201,001 , GRCh38.p12 chr3: 20,159,428-20,159,509 SGO1
    nsv4585644copy number variation1nstd183human GRCh37 chr3: 19,535,653-20,638,501 , GRCh38.p12 chr3: 19,494,161-20,597,009 , RPL39P18, 16 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
    nsv4519548copy number variation1nstd166human GRCh37.p13 chr3: 20,221,043-20,221,137 , GRCh38.p12 chr3: 20,179,551-20,179,645 SGO1, SGO1-AS1
    nsv4470464mobile element insertion1nstd166human GRCh37.p13 chr3: 20,207,068-20,207,068 , GRCh38.p12 chr3: 20,165,576-20,165,576 SGO1
    nsv4452346copy number variation1nstd102humanPathogenic GRCh37 chr3: 19,064,852-26,448,689 , GRCh38.p12 chr3: 19,023,360-26,407,198 RPL15, SGO1, 71 more genes
    nsv4451821copy number variation1nstd102humanUncertain significance GRCh37 chr3: 19,833,713-20,933,527 , GRCh38.p12 chr3: 19,792,221-20,892,035 SGO1-AS1, RNY4P22, 13 more genes
    nsv4411220copy number variation1nstd174human GRCh37 chr3: 20,200,095-20,201,582 , GRCh38.p12 chr3: 20,158,603-20,160,090 SGO1
    nsv4408229copy number variation1nstd174human GRCh37 chr3: 20,200,577-20,201,338 , GRCh38.p12 chr3: 20,159,085-20,159,846 SGO1
    nsv4087429copy number variation1nstd166human GRCh37.p13 chr3: 20,223,329-20,223,438 , GRCh38.p12 chr3: 20,181,837-20,181,946 SGO1, SGO1-AS1
    nsv4079224copy number variation1nstd166human GRCh37.p13 chr3: 20,225,000-20,230,000 , GRCh38.p12 chr3: 20,183,508-20,188,508 , SGO1-AS1, 1 more genes
    nsv4076908copy number variation1nstd166human GRCh37.p13 chr3: 19,642,494-20,205,465 , GRCh38.p12 chr3: 19,601,002-20,163,973 MIR3135A, RPL39P18, 9 more genes
    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
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