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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5905552copy number variation1nstd209human GRCh38 chr2: 241,225,222-241,225,538 , GRCh37.p13 chr2: 242,164,637-242,164,953 HDLBP, ANO7, 1 more genes
    nsv5903469copy number variation1nstd209human GRCh38 chr2: 241,264,054-241,264,120 , GRCh37.p13 chr2: 242,203,469-242,203,535 HDLBP
    nsv5901920copy number variation1nstd209human GRCh38 chr2: 241,258,569-241,258,621 , GRCh37.p13 chr2: 242,197,984-242,198,036 HDLBP
    nsv5901838copy number variation1nstd209human GRCh38 chr2: 241,281,225-241,281,391 , GRCh37.p13 chr2: 242,220,640-242,220,806 HDLBP
    nsv5889153copy number variation1nstd209human GRCh38 chr2: 241,240,403-241,241,668 , GRCh37.p13 chr2: 242,179,818-242,181,083 HDLBP
    nsv5832833copy number variation1nstd209human GRCh38 chr2: 241,240,439-241,241,638 , GRCh37.p13 chr2: 242,179,854-242,181,053 HDLBP
    nsv5689264mobile element insertion2nstd211human GRCh38 chr2: 241,264,054-241,264,054 , GRCh37.p13 chr2: 242,203,469-242,203,469 HDLBP
    nsv5605974insertion1nstd207human GRCh38 chr2: 241,264,041-241,264,041 , GRCh37.p13 chr2: 242,203,456-242,203,456 HDLBP
    nsv5545447insertion1nstd206human GRCh38 chr2: 241,241,419-241,241,447 , GRCh37.p13 chr2: 242,180,834-242,180,862 HDLBP
    nsv5449598copy number variation1nstd206human GRCh38 chr2: 241,225,242-241,225,539 , GRCh37.p13 chr2: 242,164,657-242,164,954 HDLBP, ANO7, 1 more genes
    nsv5447496copy number variation1nstd206human GRCh38 chr2: 241,235,910-241,235,972 , GRCh37.p13 chr2: 242,175,325-242,175,387 ANO7, HDLBP
    nsv5446610copy number variation1nstd206human GRCh38 chr2: 241,240,405-241,241,669 , GRCh37.p13 chr2: 242,179,820-242,181,084 HDLBP
    nsv5446599copy number variation1nstd206human GRCh38 chr2: 241,287,008-241,287,392 , GRCh37.p13 chr2: 242,226,423-242,226,807 HDLBP
    nsv5440858copy number variation1nstd206human GRCh38 chr2: 241,235,917-241,236,052 , GRCh37.p13 chr2: 242,175,332-242,175,467 ANO7, HDLBP
    nsv5439444copy number variation1nstd206human GRCh38 chr2: 241,223,783-241,225,925 , GRCh37.p13 chr2: 242,163,198-242,165,340 ANO7, LOC105376810, 1 more genes
    nsv5437490copy number variation1nstd206human GRCh38 chr2: 241,260,000-241,488,047 , GRCh37.p13 chr2: 242,199,415-242,427,462 HDLBP, SEPTIN2, 5 more genes
    nsv5408135mobile element insertion1nstd206human GRCh38 chr2: 241,264,054-241,264,063 , GRCh37.p13 chr2: 242,203,469-242,203,478 HDLBP
    nsv5381323copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,201,756-243,048,760 , GRCh38.p12 chr2: 236,293,113-242,106,609 LRRFIP1, GPR35, 133 more genes
    nsv5351296translocation1nstd200human GRCh38 chr2: 241,292,843-241,292,843 , GRCh38 chr2: 241,292,756-241,292,756 , GRCh37.p13 chr2: 242,232,258-242,232,258 , GRCh37.p13 chr2: 242,232,171-242,232,171 HDLBP
    nsv5351295translocation1nstd200human GRCh38 chr2: 241,240,405-241,240,405 , GRCh38 chr2: 241,241,669-241,241,669 , GRCh37.p13 chr2: 242,179,820-242,179,820 , GRCh37.p13 chr2: 242,181,084-242,181,084 HDLBP
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