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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5438022copy number variation1nstd206human GRCh38 chr3: 39,115,452-39,115,558 , GRCh37.p13 chr3: 39,156,943-39,157,049 TTC21A
    nsv5351673translocation1nstd200human GRCh38 chr3: 39,127,470-39,127,470 , GRCh38 chr3: 39,127,547-39,127,547 , GRCh37.p13 chr3: 39,168,961-39,168,961 , GRCh37.p13 chr3: 39,169,038-39,169,038 TTC21A
    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
    nsv4924346copy number variation1nstd200human GRCh38 chr3: 39,130,414-39,136,651 , GRCh37.p13 chr3: 39,171,905-39,178,142 TTC21A, MIR6822
    nsv4924345copy number variation1nstd200human GRCh38 chr3: 39,078,915-39,112,331 , GRCh37.p13 chr3: 39,120,406-39,153,822 TTC21A, GORASP1, 1 more genes
    nsv4910874copy number variation1nstd200human GRCh38 chr3: 39,116,990-39,117,260 , GRCh37.p13 chr3: 39,158,481-39,158,751 TTC21A
    nsv4910873copy number variation1nstd200human GRCh38 chr3: 39,115,452-39,115,558 , GRCh37.p13 chr3: 39,156,943-39,157,049 TTC21A
    nsv4910872copy number variation1nstd200human GRCh38 chr3: 39,106,538-39,108,160 , GRCh37.p13 chr3: 39,148,029-39,149,651 GORASP1, TTC21A
    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
    nsv4806639copy number variation1nstd200human GRCh37 chr3: 39,148,029-39,149,651 , GRCh38.p12 chr3: 39,106,538-39,108,160 TTC21A, GORASP1
    nsv4588564copy number variation1nstd183human GRCh37 chr3: 39,168,283-39,182,691 , GRCh38.p12 chr3: 39,126,792-39,141,200 TTC21A, MIR6822, 1 more genes
    nsv4566703mobile element insertion1nstd166human GRCh37.p13 chr3: 39,147,216-39,147,216 , GRCh38.p12 chr3: 39,105,725-39,105,725 GORASP1, TTC21A
    nsv4566516mobile element insertion1nstd166human GRCh37.p13 chr3: 39,164,941-39,164,941 , GRCh38.p12 chr3: 39,123,450-39,123,450 TTC21A
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4082601copy number variation1nstd166human GRCh37.p13 chr3: 39,180,358-39,186,491 , GRCh38.p12 chr3: 39,138,867-39,145,000 CSRNP1, TTC21A
    nsv3917642copy number variation1nstd102humanPathogenic NCBI36 chr3: 33,744,902-40,678,946 , GRCh37 chr3: 33,769,898-40,703,942 , GRCh38 chr3: 33,728,406-40,662,451 STAC, SCN11A, 111 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
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
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