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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5898260copy number variation1nstd209human GRCh38 chr5: 156,986,485-157,423,872 , GRCh37.p13 chr5: 156,413,496-156,850,880 ITK, MED7, 7 more genes
    nsv5890679copy number variation1nstd209human GRCh38 chr5: 157,083,499-157,083,960 , GRCh37.p13 chr5: 156,510,510-156,510,971 HAVCR2
    nsv5460788copy number variation1nstd206human GRCh38 chr5: 157,106,342-157,111,226 , GRCh37.p13 chr5: 156,533,353-156,538,237 HAVCR2
    nsv5456127copy number variation1nstd206human GRCh38 chr5: 157,099,446-157,099,843 , GRCh37.p13 chr5: 156,526,457-156,526,854 HAVCR2
    nsv5308470copy number variation1nstd204human GRCh38.p13 chr5: 157,101,880-157,111,315 , GRCh37.p13 chr5: 156,528,891-156,538,326 HAVCR2
    nsv5232330copy number variation1nstd204human GRCh38.p13 chr5: 157,104,201-157,111,100 , GRCh37.p13 chr5: 156,531,212-156,538,111 HAVCR2
    nsv5226651copy number variation1nstd204human GRCh38.p13 chr5: 157,103,151-157,110,560 , GRCh37.p13 chr5: 156,530,162-156,537,571 HAVCR2
    nsv5224787copy number variation1nstd204human GRCh38.p13 chr5: 157,101,701-157,111,394 , GRCh37.p13 chr5: 156,528,712-156,538,405 HAVCR2
    nsv5083777mobile element insertion1nstd203human GRCh38 chr5: 157,092,878-157,092,918 , GRCh37.p13 chr5: 156,519,889-156,519,929 HAVCR2
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4824346copy number variation1nstd200human GRCh37 chr5: 156,529,055-156,538,124 , GRCh38.p12 chr5: 157,102,044-157,111,113 HAVCR2
    nsv4674945copy number variation1nstd102humanPathogenic GRCh37 chr5: 156,347,980-169,959,880 , GRCh38.p12 chr5: 156,920,969-170,532,876 LINC02227, LINC01932, 146 more genes
    nsv4597846copy number variation1nstd183human GRCh37 chr5: 156,526,074-156,536,378 , GRCh38.p12 chr5: 157,099,063-157,109,367 HAVCR2
    nsv4592752copy number variation1nstd183human GRCh37 chr5: 156,515,406-156,523,404 , GRCh38.p12 chr5: 157,088,395-157,096,393 HAVCR2
    nsv4129776copy number variation1nstd166human GRCh37.p13 chr5: 156,522,025-156,522,090 , GRCh38.p12 chr5: 157,095,014-157,095,079 HAVCR2
    nsv4127665copy number variation1nstd166human GRCh37.p13 chr5: 156,529,095-156,538,045 , GRCh38.p12 chr5: 157,102,084-157,111,034 HAVCR2
    nsv4127471copy number variation1nstd166human GRCh37.p13 chr5: 156,522,179-156,522,286 , GRCh38.p12 chr5: 157,095,168-157,095,275 HAVCR2
    nsv4113065copy number variation1nstd166human GRCh37.p13 chr5: 156,529,995-156,530,047 , GRCh38.p12 chr5: 157,102,984-157,103,036 HAVCR2
    nsv3924400copy number variation1nstd102humanPathogenic NCBI36 chr5: 156,185,101-180,629,412 , GRCh37 chr5: 156,252,523-180,696,806 , GRCh38 chr5: 156,825,512-181,269,805 CEP192P1, ARL2BPP6, 443 more genes
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