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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5901718copy number variation1nstd209human GRCh38 chr5: 172,153,284-177,326,767 , GRCh37.p13 chr5: 171,580,288-176,753,768 , LOC107986487, 114 more genes
    nsv5894952copy number variation1nstd209human GRCh38 chr5: 175,699,062-175,699,114 , GRCh37.p13 chr5: 175,126,065-175,126,117 HRH2
    nsv5890670copy number variation1nstd209human GRCh38 chr5: 175,681,730-175,681,792 , GRCh37.p13 chr5: 175,108,733-175,108,795 HRH2
    nsv5469534copy number variation1nstd206human GRCh38 chr5: 175,681,327-175,681,413 , GRCh37.p13 chr5: 175,108,330-175,108,416 HRH2
    nsv5362715translocation1nstd200human GRCh38 chr5: 175,681,730-175,681,730 , GRCh38 chr5: 175,681,793-175,681,793 , GRCh37.p13 chr5: 175,108,796-175,108,796 , GRCh37.p13 chr5: 175,108,733-175,108,733 HRH2
    nsv5350638translocation1nstd200human GRCh38 chr5: 175,663,545-175,663,545 , GRCh38 chr1: 26,429,165-26,429,165 , GRCh37.p13 chr5: 175,090,548-175,090,548 , GRCh37.p13 chr1: 26,755,656-26,755,656 LIN28A, HRH2
    nsv5332280translocation1nstd200human GRCh37 chr5: 175,090,548-175,090,548 , GRCh37 chr1: 26,755,656-26,755,656 , GRCh38.p12 chr5: 175,663,545-175,663,545 , GRCh38.p12 chr1: 26,429,165-26,429,165 HRH2, LIN28A
    nsv5322233translocation1nstd204human GRCh38.p13 chr5: 175,681,730-175,681,730 , GRCh38.p13 chr5: 175,681,793-175,681,793 , GRCh37.p13 chr5: 175,108,796-175,108,796 , GRCh37.p13 chr5: 175,108,733-175,108,733 HRH2
    nsv5238848copy number variation1nstd204human GRCh38.p13 chr5: 175,699,026-175,700,136 , GRCh37.p13 chr5: 175,126,029-175,127,139 HRH2
    nsv4949243copy number variation1nstd200human GRCh38 chr5: 175,666,468-175,669,440 , GRCh37.p13 chr5: 175,093,471-175,096,443 HRH2
    nsv4947432copy number variation1nstd200human GRCh38 chr5: 175,707,219-175,707,336 , GRCh37.p13 chr5: 175,134,222-175,134,339 HRH2
    nsv4947431copy number variation1nstd200human GRCh38 chr5: 175,677,527-175,679,245 , GRCh37.p13 chr5: 175,104,530-175,106,248 HRH2
    nsv4825985copy number variation1nstd200human GRCh37 chr5: 175,134,222-175,134,339 , GRCh38.p12 chr5: 175,707,219-175,707,336 HRH2
    nsv4824399copy number variation1nstd200human GRCh37 chr5: 175,093,472-175,096,442 , GRCh38.p12 chr5: 175,666,469-175,669,439 HRH2
    nsv4768375copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,805,664-180,719,789 , GRCh38.p12 chr5: 171,378,660-181,292,788 LINC01863, PRDX2P3, 279 more genes
    nsv4763538inversion1nstd199human GRCh37 chr5: 170,260,689-178,183,120 , GRCh38.p12 chr5: 170,833,685-178,756,119 , BNIP1, 194 more genes
    nsv4592810copy number variation1nstd183human GRCh37 chr5: 175,085,103-175,085,162 , GRCh38.p12 chr5: 175,658,100-175,658,159 HRH2
    nsv4350559copy number variation1nstd102humanPathogenic GRCh37 chr5: 174,990,352-180,690,937 , GRCh38.p12 chr5: 175,563,349-181,263,936 FAF2, ARL10, 198 more genes
    nsv4130905copy number variation1nstd166human GRCh37.p13 chr5: 175,108,733-175,108,796 , GRCh38.p12 chr5: 175,681,730-175,681,793 HRH2
    nsv4130013copy number variation1nstd166human GRCh37.p13 chr5: 175,092,891-175,100,473 , GRCh38.p12 chr5: 175,665,888-175,673,470 HRH2
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