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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5947920copy number variation1nstd209human GRCh38 chr22: 37,164,368-37,165,011 , GRCh37.p13 chr22: 37,560,408-37,561,051 IL2RB
    nsv5887506copy number variation1nstd209human GRCh38 chr22: 37,156,814-37,158,813 , GRCh37.p13 chr22: 37,552,854-37,554,853 IL2RB
    nsv5879296copy number variation1nstd209human GRCh38 chr22: 37,151,890-37,154,389 , GRCh37.p13 chr22: 37,547,930-37,550,429 IL2RB
    nsv5541330copy number variation1nstd206human GRCh38 chr22: 37,164,371-37,165,012 , GRCh37.p13 chr22: 37,560,411-37,561,052 IL2RB
    nsv5360556translocation1nstd200human GRCh38 chr22: 37,165,012-37,165,012 , GRCh38 chr22: 37,164,371-37,164,371 , GRCh37.p13 chr22: 37,560,411-37,560,411 , GRCh37.p13 chr22: 37,561,052-37,561,052 IL2RB
    nsv5327852copy number variation1nstd204human GRCh38.p13 chr22: 37,164,341-37,165,040 , GRCh37.p13 chr22: 37,560,381-37,561,080 IL2RB
    nsv5287425copy number variation1nstd204human GRCh38.p13 chr22: 37,131,028-37,154,789 , GRCh37.p13 chr22: 37,527,068-37,550,829 IL2RB
    nsv5285762copy number variation1nstd204human GRCh38.p13 chr22: 36,751,901-37,231,800 , GRCh37.p13 chr22: 37,147,945-37,627,840 RN7SKP214, LOC105373022, 20 more genes
    nsv5281378copy number variation1nstd204human GRCh38.p13 chr22: 37,138,594-37,140,878 , GRCh37.p13 chr22: 37,534,634-37,536,918 IL2RB
    nsv4885782copy number variation1nstd200human GRCh37 chr22: 37,524,121-37,524,237 , GRCh38.p12 chr22: 37,128,081-37,128,197 IL2RB
    nsv4880151copy number variation1nstd200human GRCh37 chr22: 37,560,411-37,561,052 , GRCh38.p12 chr22: 37,164,371-37,165,012 IL2RB
    nsv4745493copy number variation1nstd199human GRCh37 chr22: 37,521,543-37,521,610 , GRCh38.p12 chr22: 37,125,503-37,125,570 IL2RB
    nsv4733842copy number variation1nstd199human GRCh37 chr22: 37,564,908-37,564,979 , GRCh38.p12 chr22: 37,168,868-37,168,939 IL2RB
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4676292copy number variation1nstd102humanPathogenic GRCh37 chr22: 30,654,764-51,197,838 , GRCh38.p12 chr22: 30,258,775-50,759,410 PDXP-DT, PDGFB, 550 more genes
    nsv4629370copy number variation1nstd183human GRCh37 chr22: 37,523,383-37,638,617 , GRCh38.p12 chr22: 37,127,343-37,242,577 C1QTNF6, IL2RB, 3 more genes
    nsv4457771copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410 IGLV3-27, XKR3, 1082 more genes
    nsv4278013copy number variation1nstd166human GRCh37.p13 chr22: 37,381,892-38,500,309 , GRCh38.p12 chr22: 36,985,851-38,104,302 GGA1, GALR3, 46 more genes
    nsv4277511copy number variation1nstd166human GRCh37.p13 chr22: 37,560,411-37,561,052 , GRCh38.p12 chr22: 37,164,371-37,165,012 IL2RB
    nsv3922128copy number variation1nstd102humanPathogenic GRCh37 chr22: 35,729,986-39,296,182 , NCBI36 chr22: 34,059,986-37,626,128 , GRCh38 chr22: 35,333,993-38,900,177 LOC102724378, CARD10, 120 more genes
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