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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5972468inversion1nstd209human GRCh37.p13 chr5: 179,064,647-179,087,095 , GRCh38 chr5: 179,637,646-179,660,094 C5orf60, LOC100502572, 1 more genes
    nsv5900893copy number variation1nstd209human GRCh38 chr5: 179,640,156-179,640,666 , GRCh37.p13 chr5: 179,067,157-179,067,667 C5orf60
    nsv5897875copy number variation1nstd209human GRCh38 chr5: 179,639,093-179,639,715 , GRCh37.p13 chr5: 179,066,094-179,066,716 C5orf60
    nsv5892721copy number variation1nstd209human GRCh38 chr5: 179,524,543-179,651,938 , GRCh37.p13 chr5: 178,951,544-179,078,939 HNRNPH1, RUFY1, 6 more genes
    nsv5842257copy number variation1nstd209human GRCh38 chr5: 179,642,912-179,659,971 , GRCh37.p13 chr5: 179,069,913-179,086,972 LOC100502572, LOC105377763, 1 more genes
    nsv5842239copy number variation1nstd209human GRCh38 chr5: 179,635,998-179,644,599 , GRCh37.p13 chr5: 179,062,999-179,071,600 C5orf60
    nsv5672210inversion1nstd207human GRCh37.p13 chr5: 179,060,844-179,085,555 , GRCh38 chr5: 179,633,843-179,658,554 HNRNPH1, C5orf60, 2 more genes
    nsv5576885copy number variation1nstd207human GRCh38 chr5: 179,640,156-179,640,666 , GRCh37.p13 chr5: 179,067,157-179,067,667 C5orf60
    nsv5561640sequence alteration1nstd206human GRCh38 chr5: 179,554,688-180,310,132 , GRCh37.p13 chr5: 178,981,689-179,737,132 LTC4S, MIR340, 28 more genes
    nsv5456838copy number variation1nstd206human GRCh38 chr5: 179,638,913-179,639,697 , GRCh37.p13 chr5: 179,065,914-179,066,698 C5orf60
    nsv5454577copy number variation1nstd206human GRCh38 chr5: 179,640,167-179,640,658 , GRCh37.p13 chr5: 179,067,168-179,067,659 C5orf60
    nsv5385701copy number variation1nstd186human GRCh37 chr5: 179,067,453-179,067,646 , GRCh38.p12 chr5: 179,640,452-179,640,645 C5orf60
    nsv5381440copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,699,902-179,263,603 , GRCh38.p12 chr5: 179,272,901-179,836,603 , GRCh38.p12 chr5|NW_016107298.1: 37,608-602,163 LOC105377762, LOC105377759, 21 more genes
    nsv5381377copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,770,758-179,263,603 , GRCh38.p12 chr5: 179,343,757-179,836,603 , GRCh38.p12 chr5|NW_016107298.1: 108,464-602,163 LOC100502572, C5orf60, 21 more genes
    nsv5362744translocation1nstd200human GRCh38 chr5: 179,639,697-179,639,697 , GRCh38 chr5: 179,639,112-179,639,112 , GRCh37.p13 chr5: 179,066,113-179,066,113 , GRCh37.p13 chr5: 179,066,698-179,066,698 C5orf60
    nsv5336055translocation1nstd200human GRCh37 chr5: 179,080,409-179,080,409 , GRCh37 chr5: 179,068,309-179,068,309 , GRCh38.p12 chr5|NW_016107298.1: 417,456-417,456 , GRCh38.p12 chr5: 179,641,308-179,641,308 , GRCh38.p12 chr5: 179,653,408-179,653,408 , GRCh38.p12 chr5|NW_016107298.1: 405,366-405,366 C5orf60, LOC100502572
    nsv5309377copy number variation1nstd204human GRCh38.p13 chr5: 179,640,167-179,640,658 , GRCh37.p13 chr5: 179,067,168-179,067,659 C5orf60
    nsv5303183copy number variation1nstd204human GRCh38.p13 chr5: 179,639,085-179,639,718 , GRCh37.p13 chr5: 179,066,086-179,066,719 C5orf60
    nsv5301596copy number variation1nstd204human GRCh38.p13 chr5: 179,616,292-180,442,361 , GRCh37.p13 chr5: 179,043,293-179,869,361 MIR1229, MAPK9, 25 more genes
    nsv5233947copy number variation1nstd204human GRCh38.p13 chr5: 179,616,201-179,907,500 , GRCh37.p13 chr5: 179,043,202-179,334,500 CBY3, LOC100502572, 15 more genes
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