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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
    nsv5473852copy number variation1nstd206human GRCh38 chr5: 172,959,073-172,962,703 , GRCh37.p13 chr5: 172,386,076-172,389,706 RPL26L1-AS1, RPL26L1
    nsv5236809copy number variation1nstd204human GRCh38.p13 chr5: 172,787,101-172,974,900 , GRCh37.p13 chr5: 172,214,104-172,401,903 RPL26L1-AS1, ERGIC1, 3 more genes
    nsv5095743mobile element insertion1nstd203human GRCh38 chr5: 172,966,122-172,966,135 , GRCh37.p13 chr5: 172,393,125-172,393,138 RPL26L1
    nsv4947330copy number variation1nstd200human GRCh38 chr5: 172,959,101-172,962,661 , GRCh37.p13 chr5: 172,386,104-172,389,664 RPL26L1, RPL26L1-AS1
    nsv4947329copy number variation1nstd200human GRCh38 chr5: 172,956,884-172,959,095 , GRCh37.p13 chr5: 172,383,887-172,386,098 RPL26L1, RPL26L1-AS1
    nsv4947328copy number variation1nstd200human GRCh38 chr5: 172,953,099-172,958,811 , GRCh37.p13 chr5: 172,380,102-172,385,814 RPL26L1-AS1, ERGIC1, 1 more genes
    nsv4939965copy number variation1nstd200human GRCh38 chr5: 172,969,379-172,975,474 , GRCh37.p13 chr5: 172,396,382-172,402,477 LOC285591, RPL26L1
    nsv4939964copy number variation1nstd200human GRCh38 chr5: 172,968,811-172,977,803 , GRCh37.p13 chr5: 172,395,814-172,404,806 RPL26L1, LOC285591
    nsv4825924copy number variation1nstd200human GRCh37 chr5: 172,395,814-172,404,808 , GRCh38.p12 chr5: 172,968,811-172,977,805 RPL26L1, LOC285591
    nsv4825923copy number variation1nstd200human GRCh37 chr5: 172,386,110-172,389,670 , GRCh38.p12 chr5: 172,959,107-172,962,667 RPL26L1-AS1, RPL26L1
    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
    nsv4578263copy number variation1nstd102humanPathogenic GRCh37 chr5: 166,420,934-173,324,844 , GRCh38.p12 chr5: 166,993,929-173,897,841 LINC01187, TENM2-AS1, 112 more genes
    nsv4547372insertion1nstd166human GRCh37.p13 chr5: 172,393,125-172,393,125 , GRCh38.p12 chr5: 172,966,122-172,966,122 RPL26L1
    nsv4522379copy number variation1nstd166human GRCh37.p13 chr5: 172,393,994-172,394,045 , GRCh38.p12 chr5: 172,966,991-172,967,042 RPL26L1
    nsv4132308copy number variation1nstd166human GRCh37.p13 chr5: 172,380,103-172,385,826 , GRCh38.p12 chr5: 172,953,100-172,958,823 ERGIC1, RPL26L1, 1 more genes
    nsv4124575copy number variation1nstd166human GRCh37.p13 chr5: 172,386,083-172,389,772 , GRCh38.p12 chr5: 172,959,080-172,962,769 RPL26L1, RPL26L1-AS1
    nsv4123865copy number variation1nstd166human GRCh37.p13 chr5: 171,633,200-172,488,112 , GRCh38.p12 chr5: 172,206,196-173,061,109 CREBRF, RPL26L1, 23 more genes
    nsv4114448copy number variation1nstd166human GRCh37.p13 chr5: 172,395,814-172,404,806 , GRCh38.p12 chr5: 172,968,811-172,977,803 RPL26L1, LOC285591
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