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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2676574copy number variation189estd199human GRCh37 chr6: 78,967,194-79,036,497 , GRCh38.p12 chr6: 78,257,477-78,326,780 LOC105377865
    esv2666739copy number variation325estd199human GRCh37 chr1: 207,699,545-207,737,892 , GRCh38.p12 chr1: 207,526,200-207,564,547 CR1
    esv2668226copy number variation311estd199human GRCh37 chr3: 129,763,245-129,799,692 , GRCh38.p12 chr3: 130,044,402-130,080,849 ALG1L2
    esv2673583copy number variation519estd199human GRCh37 chr20: 1,560,991-1,594,041 , GRCh38.p12 chr20: 1,580,345-1,613,395 SIRPB1
    esv2669475copy number variation624estd199human GRCh37 chr1: 147,976,045-147,996,192 , GRCh38.p12 chr1: 120,848,940-120,869,086 RNVU1-19
    esv2663133copy number variation46estd199human GRCh37 chr6: 32,629,745-32,648,392 , GRCh38.p12 chr6: 32,661,968-32,680,615 HLA-DQB1
    esv2674647copy number variation204estd199human GRCh37 chr8: 56,377,729-56,393,641 , GRCh38.p12 chr8: 55,465,169-55,481,081 XKR4
    esv2669960copy number variation208estd199human GRCh37 chr9: 41,968,745-41,984,492 , GRCh38.p12 chr9: 39,823,727-39,839,474 FGF7P3
    esv2664803copy number variation436estd199human GRCh37 chr15: 76,884,596-76,896,938 , GRCh38.p12 chr15: 76,592,255-76,604,597 SCAPER
    esv2678677copy number variation179estd199human GRCh37 chr15: 76,884,295-76,895,742 , GRCh38.p12 chr15: 76,591,954-76,603,401 SCAPER
    esv2657260copy number variation826estd199human GRCh37 chr2: 87,730,745-87,740,792 , GRCh38.p12 chr2: 87,431,226-87,441,083 LINC01943
    esv2662536copy number variation311estd199human GRCh37 chr6: 72,863,851-72,873,540 , GRCh38.p12 chr6: 72,154,148-72,163,837 RIMS1
    esv2661768copy number variation445estd199human GRCh37 chr5: 12,811,019-12,820,535 , GRCh38.p12 chr5: 12,810,907-12,820,423 LOC105374657
    esv2665039copy number variation13estd199human GRCh37 chr21: 28,450,960-28,459,835 , GRCh38.p12 chr21: 27,078,641-27,087,516
    esv2668940copy number variation193estd199human GRCh37 chr12: 99,793,947-99,802,770 , GRCh38.p12 chr12: 99,400,169-99,408,992 ANKS1B
    esv2673043copy number variation328estd199human GRCh37 chr14: 80,106,288-80,115,049 , GRCh38.p12 chr14: 79,639,945-79,648,706 NRXN3
    esv2663931copy number variation243estd199human GRCh37 chr4: 138,092,000-138,100,631 , GRCh38.p12 chr4: 137,170,846-137,179,477 LINC02511
    esv2677597copy number variation57estd199human GRCh37 chr15: 100,414,545-100,422,992 , GRCh38.p12 chr15: 99,874,340-99,882,787 LOC400464
    esv2658675copy number variation40estd199human GRCh37 chr1: 222,373,295-222,381,692 , GRCh38.p12 chr1: 222,199,953-222,208,350 CFAP144P3
    esv2678804copy number variation26estd199human GRCh37 chr12: 99,793,445-99,801,692 , GRCh38.p12 chr12: 99,399,667-99,407,914 ANKS1B
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