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Items: 1 to 20 of 83

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4073804copy number variation1nstd166human GRCh37.p13 chr3: 23,232,081-23,245,284 , GRCh38.p12 chr3: 23,190,590-23,203,793 UBE2E2-DT, UBE2E2
    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
    nsv3923353copy number variation1nstd102humanPathogenic GRCh38 chr3: 19,915,382-25,537,973 , GRCh37 chr3: 19,956,874-25,579,464 , NCBI36 chr3: 19,931,878-25,554,468 RNU6-822P, UBE2E1-AS1, 52 more genes
    nsv3919171copy number variation1nstd102humanPathogenic NCBI36 chr3: 20,070,947-23,875,231 , GRCh37 chr3: 20,095,943-23,900,227 , GRCh38 chr3: 20,054,451-23,858,736 RRBP1P2, UBE2E1, 25 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
    nsv3901059copy number variation1nstd102humanPathogenic GRCh37 chr3: 73,914-30,105,699 , GRCh38 chr3: 32,241-30,064,208 , NCBI36 chr3: 48,914-30,080,703 RPL32, RPL15, 369 more genes
    nsv3892895copy number variation1nstd102humanPathogenic GRCh38 chr3: 52,266-37,148,076 , GRCh37 chr3: 93,949-37,189,567 , NCBI36 chr3: 68,949-37,164,571 RPL34P11, RNU1-96P, 452 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
    nsv3888298copy number variation1nstd102humanPathogenic GRCh37 chr3: 13,276,005-24,295,240 , GRCh38.p12 chr3: 13,234,505-24,253,749 NR1D2, RRBP1P2, 134 more genes
    nsv3886409copy number variation1nstd102humanBenign GRCh37 chr3: 22,833,287-23,236,703 , GRCh38.p12 chr3: 22,791,796-23,195,212 SALL4P5, RANP7, 3 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
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