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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958558insertion1nstd209human GRCh38 chr3: 43,700,732-43,700,732 , GRCh37.p13 chr3: 43,742,224-43,742,224 ABHD5
    nsv5615639insertion1nstd207human GRCh38 chr3: 43,700,732-43,700,732 , GRCh37.p13 chr3: 43,742,224-43,742,224 ABHD5
    nsv5553420insertion1nstd206human GRCh38 chr3: 43,700,652-43,700,740 , GRCh37.p13 chr3: 43,742,144-43,742,232 ABHD5
    nsv5066477mobile element insertion1nstd203human GRCh38 chr3: 43,694,068-43,694,068 , GRCh37.p13 chr3: 43,735,560-43,735,560 ABHD5
    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
    nsv4924376copy number variation1nstd200human GRCh38 chr3: 43,715,412-43,726,157 , GRCh37.p13 chr3: 43,756,904-43,767,649 ABHD5
    nsv4911028copy number variation1nstd200human GRCh38 chr3: 43,720,336-43,724,877 , GRCh37.p13 chr3: 43,761,828-43,766,369 ABHD5
    nsv4911027copy number variation1nstd200human GRCh38 chr3: 43,697,689-43,698,776 , GRCh37.p13 chr3: 43,739,181-43,740,268 ABHD5
    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
    nsv4793952copy number variation1nstd200human GRCh37 chr3: 43,756,904-43,767,649 , GRCh38.p12 chr3: 43,715,412-43,726,157 ABHD5
    nsv4790474copy number variation1nstd200human GRCh37 chr3: 43,761,828-43,766,369 , GRCh38.p12 chr3: 43,720,336-43,724,877 ABHD5
    nsv4790473copy number variation1nstd200human GRCh37 chr3: 43,739,181-43,740,268 , GRCh38.p12 chr3: 43,697,689-43,698,776 ABHD5
    nsv4756245insertion1nstd199human GRCh37 chr3: 43,742,229-43,742,229 , GRCh38.p12 chr3: 43,700,737-43,700,737 ABHD5
    nsv4728435copy number variation1nstd102humanUncertain significance GRCh37 chr3: 43,230,722-43,933,855 , GRCh38.p12 chr3: 43,189,230-43,892,363 LOC105377052, ANO10, 7 more genes
    nsv4723938insertion1nstd186human GRCh37 chr3: 43,735,560-43,735,560 , GRCh38.p12 chr3: 43,694,068-43,694,068 ABHD5
    nsv4722224insertion1nstd186human GRCh37 chr3: 43,742,224-43,742,224 , GRCh38.p12 chr3: 43,700,732-43,700,732 ABHD5
    nsv4661944copy number variation1nstd186human GRCh37 chr3: 43,731,904-43,733,080 , GRCh38.p12 chr3: 43,690,412-43,691,588 ABHD5, ANO10
    nsv4596478copy number variation1nstd183human GRCh37 chr3: 43,731,904-43,733,080 , GRCh38.p12 chr3: 43,690,412-43,691,588 ABHD5, ANO10
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