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Items: 1 to 20 of 562

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5669609inversion1nstd207human GRCh37.p13 chr5: 68,918,003-70,295,816 , GRCh38 chr5: 69,622,176-70,999,989 , CDH12P2, 36 more genes
    nsv5575411copy number variation1nstd207human GRCh38 chr5: 70,042,238-70,044,949 , GRCh37.p13 chr5: 69,338,065-69,340,776 LOC107986372, SERF1B
    nsv5237328copy number variation1nstd204human GRCh38.p13 chr5: 70,034,101-70,041,400 , GRCh37.p13 chr5: 69,329,928-69,337,227 SERF1B, LOC107986372
    nsv5235292copy number variation1nstd204human GRCh37.p13 chr5: 69,253,428-69,497,127 , GRCh38.p13 chr5: 69,957,601-70,201,300 , CDH12P2, 7 more genes
    nsv5234315copy number variation1nstd204human GRCh38.p13 chr5: 70,019,801-70,049,100 , GRCh37.p13 chr5: 69,315,628-69,344,927 SERF1B, SMN2, 1 more genes
    nsv5232651copy number variation1nstd204human GRCh38.p13 chr5: 70,028,301-70,029,900 , GRCh37.p13 chr5: 69,324,128-69,325,727 SERF1B
    nsv5232298copy number variation1nstd204human GRCh38.p13 chr5: 70,032,601-70,034,600 , GRCh37.p13 chr5: 69,328,428-69,330,427 SERF1B
    nsv5231963copy number variation1nstd204human GRCh38.p13 chr5: 70,040,901-70,045,600 , GRCh37.p13 chr5: 69,336,728-69,341,427 LOC107986372, SERF1B
    nsv5231785copy number variation1nstd204human GRCh38.p13 chr5: 70,040,701-70,042,200 , GRCh37.p13 chr5: 69,336,528-69,338,027 LOC107986372, SERF1B
    nsv5230795copy number variation1nstd204human GRCh38.p13 chr5: 70,034,301-70,045,800 , GRCh37.p13 chr5: 69,330,128-69,341,627 LOC107986372, SERF1B
    nsv5230026copy number variation1nstd204human GRCh38.p13 chr5: 70,019,801-70,032,600 , GRCh37.p13 chr5: 69,315,628-69,328,427 SERF1B
    nsv5228135copy number variation1nstd204human GRCh38.p13 chr5: 70,019,801-70,032,300 , GRCh37.p13 chr5: 69,315,628-69,328,127 SERF1B
    nsv5227994copy number variation1nstd204human GRCh38.p13 chr5: 70,028,101-70,049,600 , GRCh37.p13 chr5: 69,323,928-69,345,427 LOC107986372, SMN2, 1 more genes
    nsv5227671copy number variation1nstd204human GRCh38.p13 chr5: 70,006,401-70,089,500 , GRCh37.p13 chr5: 69,302,228-69,385,327 LOC107986372, SMN2, 1 more genes
    nsv5227086copy number variation1nstd204human GRCh38.p13 chr5: 69,916,201-70,201,300 , GRCh37.p13 chr5: 69,212,028-69,497,127 , GUSBP14, 8 more genes
    nsv5225058copy number variation1nstd204human GRCh38.p13 chr5: 70,043,501-70,045,800 , GRCh37.p13 chr5: 69,339,328-69,341,627 SERF1B, LOC107986372
    nsv5224625copy number variation1nstd204human GRCh38.p13 chr5: 70,028,101-70,033,600 , GRCh37.p13 chr5: 69,323,928-69,329,427 SERF1B
    nsv5221688copy number variation1nstd204human GRCh38.p13 chr5: 70,039,501-70,049,100 , GRCh37.p13 chr5: 69,335,328-69,344,927 SERF1B, SMN2, 1 more genes
    nsv4730269inversion4nstd198human GRCh37.p13 chr5: 69,195,367-69,511,051 , GRCh38 chr5: 69,899,540-70,215,224 , CDH12P2, 11 more genes
    nsv4729532copy number variation1nstd102humanUncertain significance GRCh37 chr5: 68,831,650-70,663,428 , GRCh38.p12 chr5: 69,535,823-71,367,601 , GRCh38.p12 chr5|NW_003315917.2: 318,767-1,366,104 LOC105379025, GUSBP17, 52 more genes
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