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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969899inversion1nstd209human GRCh37.p13 chr3: 42,023,003-42,386,307 , GRCh38 chr3: 41,981,511-42,344,815 CCK, TRAK1, 6 more genes
    nsv5447652copy number variation1nstd206human GRCh38 chr3: 42,258,353-42,258,434 , GRCh37.p13 chr3: 42,299,845-42,299,926 CCK
    nsv5330079translocation1nstd200human GRCh37 chr3: 42,263,929-42,263,929 , GRCh37 chr3: 42,307,739-42,307,739 , GRCh38.p12 chr3: 42,222,437-42,222,437 , GRCh38.p12 chr3: 42,266,247-42,266,247 CCK, TRAK1, 1 more genes
    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
    nsv5306776copy number variation1nstd204human GRCh38.p13 chr3: 42,061,773-42,288,970 , GRCh37.p13 chr3: 42,103,265-42,330,462 CCK, LOC105377048, 3 more genes
    nsv5218719copy number variation1nstd204human GRCh38.p13 chr3: 42,259,542-42,262,012 , GRCh37.p13 chr3: 42,301,034-42,303,504 CCK
    nsv5211233copy number variation1nstd204human GRCh38.p13 chr3: 42,257,142-42,258,141 , GRCh37.p13 chr3: 42,298,634-42,299,633 CCK
    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
    nsv5167255mobile element insertion1nstd203human GRCh38 chr3: 42,257,631-42,257,645 , GRCh37.p13 chr3: 42,299,123-42,299,137 CCK
    nsv5076530mobile element insertion1nstd203human GRCh38 chr3: 42,264,128-42,264,136 , GRCh37.p13 chr3: 42,305,620-42,305,628 CCK
    nsv5066271mobile element insertion1nstd203human GRCh38 chr3: 42,264,123-42,264,136 , GRCh37.p13 chr3: 42,305,615-42,305,628 CCK
    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
    nsv4924367copy number variation1nstd200human GRCh38 chr3: 42,061,783-42,288,961 , GRCh37.p13 chr3: 42,103,275-42,330,453 TRAK1, RNU4-78P, 3 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
    nsv4793946copy number variation1nstd200human GRCh37 chr3: 42,103,275-42,330,453 , GRCh38.p12 chr3: 42,061,783-42,288,961 RNU4-78P, TPMTP2, 3 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
    nsv4471634mobile element insertion1nstd166human GRCh37.p13 chr3: 42,305,628-42,305,628 , GRCh38.p12 chr3: 42,264,136-42,264,136 CCK
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