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Items: 1 to 20 of 94

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7041966inversion1nstd229human GRCh38 chr3: 22,554,268-23,302,616 , GRCh37.p13 chr3: 22,595,759-23,344,107 RANP7, SALL4P5, 4 more genes
    nsv6718014copy number variation1nstd229human GRCh38 chr3: 23,196,801-23,198,500 , GRCh37.p13 chr3: 23,238,292-23,239,991 UBE2E2-DT
    nsv6715852copy number variation1nstd229human GRCh38 chr3: 23,191,495-23,193,831 , GRCh37.p13 chr3: 23,232,986-23,235,322 UBE2E2-DT
    nsv6710655copy number variation1nstd229human GRCh38 chr3: 23,190,590-23,203,789 , GRCh37.p13 chr3: 23,232,081-23,245,280 UBE2E2, UBE2E2-DT
    nsv6702970copy number variation1nstd229human GRCh38 chr3: 23,184,193-23,194,235 , GRCh37.p13 chr3: 23,225,684-23,235,726 UBE2E2-DT
    nsv6701136copy number variation1nstd229human GRCh38 chr3: 23,181,262-23,202,696 , GRCh37.p13 chr3: 23,222,753-23,244,187 UBE2E2-DT, UBE2E2
    nsv6699630copy number variation1nstd229human GRCh38 chr3: 23,196,012-23,220,290 , GRCh37.p13 chr3: 23,237,503-23,261,781 UBE2E2-DT, UBE2E2
    nsv6634367copy number variation1nstd102humanPathogenic GRCh37 chr3: 13,836,340-25,357,427 , GRCh38.p12 chr3: 13,794,843-25,315,936 TMEM43, SLC6A6, 132 more genes
    nsv6361959copy number variation1nstd223human GRCh38 chr3: 23,193,347-23,376,385 , GRCh37.p13 chr3: 23,234,838-23,417,876 UBE2E2-DT, UBE2E2
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 LOC102724104, CRIP1P2, 291 more genes
    nsv6135011copy number variation1nstd213human GRCh37 chr3: 23,210,000-24,090,001 , GRCh38.p12 chr3: 23,168,509-24,048,510 RPL15, UBE2E1, 9 more genes
    nsv5438615copy number variation1nstd206human GRCh38 chr3: 23,195,548-23,196,304 , GRCh37.p13 chr3: 23,237,039-23,237,795 UBE2E2-DT
    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
    nsv4924252copy number variation1nstd200human GRCh38 chr3: 23,193,347-23,376,387 , GRCh37.p13 chr3: 23,234,838-23,417,878 UBE2E2-DT, UBE2E2
    nsv4924251copy number variation1nstd200human GRCh38 chr3: 23,190,590-23,203,793 , GRCh37.p13 chr3: 23,232,081-23,245,284 UBE2E2-DT, UBE2E2
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4793887copy number variation1nstd200human GRCh37 chr3: 23,234,838-23,417,878 , GRCh38.p12 chr3: 23,193,347-23,376,387 UBE2E2-DT, UBE2E2
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    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
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