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Items: 1 to 20 of 26

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3874587copy number variation1nstd102humanBenign GRCh37 chr3: 23,513,859-23,521,204 , GRCh38.p12 chr3: 23,472,368-23,479,713 UBE2E2
    nsv3881285copy number variation1nstd102humanBenign GRCh37 chr3: 23,511,338-23,518,372 , GRCh38.p12 chr3: 23,469,847-23,476,881 UBE2E2
    nsv3889824copy number variation1nstd102humanBenign GRCh37 chr3: 23,515,901-23,521,204 , GRCh38.p12 chr3: 23,474,410-23,479,713 UBE2E2
    nsv3871131copy number variation1nstd102humanBenign GRCh37 chr3: 23,513,859-23,518,372 , GRCh38.p12 chr3: 23,472,368-23,476,881 UBE2E2
    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
    nsv4674504copy number variation1nstd102humanLikely benign GRCh37 chr3: 23,369,930-23,719,801 , GRCh38.p12 chr3: 23,328,439-23,678,310 UBE2E2, LOC105376993, 2 more genes
    nsv3875489copy number variation1nstd102humanBenign GRCh37 chr3: 23,373,052-23,713,820 , GRCh38.p12 chr3: 23,331,561-23,672,329 UBE2E2, RNU6-788P, 2 more genes
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 UBE2E2, LOC102724104, 291 more genes
    nsv4452346copy number variation1nstd102humanPathogenic GRCh37 chr3: 19,064,852-26,448,689 , GRCh38.p12 chr3: 19,023,360-26,407,198 UBE2E2, RPL15, 71 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 UBE2E2, RRBP1P2, 25 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 UBE2E2, RNU4-62P, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 UBE2E2, NDUFB4, 2876 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 UBE2E2, RPL23AP49, 2875 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 UBE2E2, LINC02022, 540 more genes
    nsv3876280copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-37,459,464 , GRCh38.p12 chr3: 20,213-37,417,973 UBE2E2, OXTR, 460 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 UBE2E2, RPL34P11, 452 more genes
    nsv3878718copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-36,710,181 , GRCh38.p12 chr3: 20,213-36,668,690 UBE2E2, LRRC3B, 436 more genes
    nsv3875913copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-33,958,201 , GRCh38.p12 chr3: 20,213-33,916,709 UBE2E2, RPS27P11, 424 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 UBE2E2, RPL32, 369 more genes
    nsv3885169copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,923,595-45,249,923 , GRCh38.p12 chr3: 16,884,818-45,208,431 UBE2E2, RNU6-243P, 382 more genes
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