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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5558385sequence alteration1nstd206human GRCh38 chr20: 47,904,922-48,493,763 , GRCh37.p13 chr20: 46,533,666-47,122,009 , LINC01523, 13 more genes
    nsv5521087copy number variation1nstd206human GRCh38 chr20: 48,128,625-48,518,625 , GRCh37.p13 chr20: 46,757,368-47,135,163 LINC00494, LOC105372641, 5 more genes
    nsv5324339inversion1nstd204human GRCh37.p13 chr20: 46,523,341-47,133,374 , GRCh38.p13 chr20: 47,894,597-48,516,210 , LINC01522, 15 more genes
    nsv5025668copy number variation1nstd200human GRCh38 chr20: 47,847,335-48,491,027 , GRCh37.p13 chr20: 46,476,079-47,119,273 , LOC107985439, 15 more genes
    nsv4762997inversion1nstd199human GRCh37 chr20: 46,523,463-47,131,459 , GRCh38.p12 chr20: 47,894,719-48,503,213 , LINC00494, 15 more genes
    nsv4679265copy number variation1nstd189human GRCh37.p13 chr20: 46,465,898-47,117,776 , GRCh38.p12 chr20: 47,837,154-48,489,530 , SRMP1, 16 more genes
    nsv4624445copy number variation1nstd183human GRCh37 chr20: 46,465,897-47,117,321 , GRCh38.p12 chr20: 47,837,153-48,489,075 , LOC107985436, 16 more genes
    nsv4498776mobile element insertion1nstd166human GRCh37.p13 chr20: 46,996,530-46,996,530 , GRCh38.p12 chr20: 48,367,787-48,367,787 LINC00494
    nsv4423874copy number variation1nstd174human GRCh37 chr20: 46,291,954-47,120,180 , GRCh38.p12 chr20: 47,663,210-48,491,934 , RNU7-173P, 19 more genes
    nsv4423696copy number variation1nstd174human GRCh37 chr20: 46,754,167-47,131,745 , GRCh38.p12 chr20: 48,125,424-48,503,499 LINC00494, LOC105372640, 6 more genes
    nsv4417298copy number variation1nstd174human GRCh37 chr20: 46,465,897-47,119,981 , GRCh38.p12 chr20: 47,837,153-48,491,735 , RNA5SP486, 16 more genes
    nsv4283412copy number variation1nstd166human GRCh37.p13 chr20: 46,994,774-46,994,856 , GRCh38.p12 chr20: 48,366,031-48,366,113 LINC00494
    nsv3924064copy number variation1nstd102humanLikely benign GRCh37 chr20: 46,478,771-47,131,081 , GRCh38 chr20: 47,850,027-48,502,835 , NCBI36 chr20: 45,912,178-46,564,488 LOC105372637, LOC105372641, 15 more genes
    nsv3921257copy number variation1nstd102humanUncertain significance GRCh38 chr20: 47,810,469-48,502,835 , GRCh37 chr20: 46,439,213-47,131,081 , NCBI36 chr20: 45,872,620-46,564,488 LOC107985436, RNU7-144P, 17 more genes
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
    nsv3918032copy number variation1nstd102humanLikely benign NCBI36 chr20: 45,872,766-46,598,326 , GRCh37.p13 chr20: 46,439,359-47,164,919 , GRCh38.p12 chr20: 47,810,615-48,548,381 RNA5SP486, LOC105372645, 18 more genes
    nsv3916996copy number variation2nstd102humanUncertain significance, conflicting data from submitters NCBI36 chr20: 45,920,755-46,541,876 , GRCh37 chr20: 46,487,348-47,108,469 , GRCh38 chr20: 47,858,604-48,480,223 LOC105372640, RNU7-92P, 13 more genes
    nsv3915005copy number variation1nstd102humanPathogenic NCBI36 chr20: 42,849,759-62,379,118 , GRCh37 chr20: 43,416,345-62,908,674 , GRCh38 chr20: 44,787,704-64,277,321 FTLP1, RNA5SP487, 472 more genes
    nsv3912430copy number variation1nstd102humanBenign GRCh37 chr20: 46,494,494-47,131,037 , NCBI36 chr20: 45,927,901-46,564,444 , GRCh38 chr20: 47,865,750-48,502,791 LOC105372637, LOC105372643, 14 more genes
    nsv3910818copy number variation1nstd102humanUncertain significance NCBI36 chr20: 25,616,026-62,435,964 , GRCh37.p13 chr20: 25,668,026-62,965,520 , GRCh38.p12 chr20: 25,687,390-64,334,167 RNA5SP481, LOC105372625, 855 more genes
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