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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5880894copy number variation1nstd209human GRCh38 chr1: 113,034,523-113,036,249 , GRCh37.p13 chr1: 113,577,145-113,578,871 LRIG2-DT
    nsv5877230copy number variation1nstd209human GRCh38 chr1: 113,018,750-113,020,632 , GRCh37.p13 chr1: 113,561,372-113,563,254 LRIG2-DT
    nsv5869829copy number variation1nstd209human GRCh38 chr1: 113,028,436-113,028,492 , GRCh37.p13 chr1: 113,571,058-113,571,114 LRIG2-DT
    nsv5827811copy number variation1nstd209human GRCh38 chr1: 113,034,884-113,036,212 , GRCh37.p13 chr1: 113,577,506-113,578,834 LRIG2-DT
    nsv5827810copy number variation1nstd209human GRCh38 chr1: 113,018,648-113,020,547 , GRCh37.p13 chr1: 113,561,270-113,563,169 LRIG2-DT
    nsv5681759mobile element insertion1nstd211human GRCh38 chr1: 113,022,582-113,022,582 , GRCh37.p13 chr1: 113,565,204-113,565,204 LRIG2-DT
    nsv5675199mobile element insertion1nstd211human GRCh38 chr1: 113,029,764-113,029,764 , GRCh37.p13 chr1: 113,572,386-113,572,386 LRIG2-DT
    nsv5622065insertion1nstd207human GRCh38 chr1: 113,070,316-113,070,316 , GRCh37.p13 chr1: 113,612,938-113,612,938 LRIG2-DT
    nsv5584113copy number variation1nstd207human GRCh38 chr1: 113,034,544-113,036,186 , GRCh37.p13 chr1: 113,577,166-113,578,808 LRIG2-DT
    nsv5571110copy number variation1nstd207human GRCh38 chr1: 113,070,089-113,070,138 , GRCh37.p13 chr1: 113,612,711-113,612,760 LRIG2-DT
    nsv5569696copy number variation1nstd207human GRCh38 chr1: 113,068,700-113,071,154 , GRCh37.p13 chr1: 113,611,322-113,613,776 LRIG2-DT
    nsv5545143insertion1nstd206human GRCh38 chr1: 113,029,734-113,029,739 , GRCh37.p13 chr1: 113,572,356-113,572,361 LRIG2-DT
    nsv5429748copy number variation1nstd206human GRCh38 chr1: 113,033,377-113,036,300 , GRCh37.p13 chr1: 113,575,999-113,578,922 LRIG2-DT
    nsv5429360copy number variation1nstd206human GRCh38 chr1: 111,687,835-115,150,000 , GRCh37.p13 chr1: 112,230,457-115,692,621 , ST7L, 77 more genes
    nsv5428108copy number variation1nstd206human GRCh38 chr1: 113,068,697-113,071,175 , GRCh37.p13 chr1: 113,611,319-113,613,797 LRIG2, LRIG2-DT
    nsv5423606copy number variation1nstd206human GRCh38 chr1: 113,025,900-113,035,389 , GRCh37.p13 chr1: 113,568,522-113,578,011 LRIG2-DT
    nsv5393694mobile element deletion2nstd186human GRCh37 chr1: 113,611,339-113,613,777 , GRCh38.p12 chr1: 113,068,717-113,071,155 LRIG2-DT
    nsv5381058copy number variation1nstd102humanPathogenic GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855 AMYP1, MIR4256, 320 more genes
    nsv5377388translocation1nstd200human GRCh38 chr1: 113,068,259-113,068,259 , GRCh38 chr1: 44,601,812-44,601,812 , GRCh37.p13 chr1: 45,067,484-45,067,484 , GRCh37.p13 chr1: 113,610,881-113,610,881 RNF220, LRIG2-DT
    nsv5363346translocation1nstd200human GRCh38 chr1: 113,068,404-113,068,404 , GRCh38 chr22: 29,591,224-29,591,224 , GRCh37.p13 chr22: 29,987,213-29,987,213 , GRCh37.p13 chr1: 113,611,026-113,611,026 LRIG2-DT
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