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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5828385copy number variation2nstd209human GRCh38 chr1: 161,551,180-161,552,877 , GRCh37.p13 chr1: 161,520,970-161,522,667 FCGR3A
    nsv5828384copy number variation2nstd209human GRCh38 chr1: 161,548,667-161,550,118 , GRCh37.p13 chr1: 161,518,457-161,519,908 FCGR3A
    nsv5828181copy number variation2nstd209human GRCh38 chr1: 161,544,051-161,547,407 , GRCh37.p13 chr1: 161,513,841-161,517,197 FCGR3A
    nsv5828066copy number variation2nstd209human GRCh38 chr1: 161,541,949-161,547,407 , GRCh37.p13 chr1: 161,511,739-161,517,197 FCGR3A
    nsv5828065copy number variation2nstd209human GRCh38 chr1: 161,528,578-161,543,022 , GRCh37.p13 chr1: 161,498,368-161,512,812 TRG-TCC2-6, TRN-GTT1-1, 3 more genes
    nsv5574494copy number variation1nstd207human GRCh38 chr1: 161,545,579-161,545,654 , GRCh37.p13 chr1: 161,515,369-161,515,444 FCGR3A
    nsv5416002copy number variation1nstd206human GRCh38 chr1: 161,514,587-161,571,793 , GRCh37.p13 chr1: 161,484,377-161,541,583 FCGR2A, FCGR3A, 7 more genes
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5378844translocation1nstd200human GRCh38 chr1: 161,540,200-161,540,200 , GRCh38 chr1: 161,621,601-161,621,601 , GRCh37.p13 chr1: 161,509,990-161,509,990 , GRCh37.p13 chr1: 161,591,391-161,591,391 FCGR3A, FCGR3B, 1 more genes
    nsv5220371copy number variation1nstd204human GRCh38.p13 chr1: 161,528,680-161,547,507 , GRCh37.p13 chr1: 161,498,470-161,517,297 TRN-GTT1-1, TRG-TCC2-6, 3 more genes
    nsv5218160copy number variation1nstd204human GRCh37.p13 chr1: 161,484,991-161,517,290 , GRCh38.p13 chr1: 161,515,201-161,547,500 FCGR2A, FCGR3A, 7 more genes
    nsv5217216copy number variation1nstd204human GRCh38.p13 chr1: 161,547,743-161,550,118 , GRCh37.p13 chr1: 161,517,533-161,519,908 FCGR3A
    nsv5216893copy number variation1nstd204human GRCh38.p13 chr1: 161,514,701-161,596,100 , GRCh37.p13 chr1: 161,484,491-161,565,890 TRN-GTT1-1, FCGR2A, 8 more genes
    nsv5216734copy number variation1nstd204human GRCh38.p13 chr1: 161,551,080-161,564,011 , GRCh37.p13 chr1: 161,520,870-161,533,801 FCGR3A
    nsv5216350copy number variation1nstd204human GRCh37.p13 chr1: 161,488,563-161,515,593 , GRCh38.p13 chr1: 161,518,773-161,545,803 FCGR2A, FCGR3A, 7 more genes
    nsv5215861copy number variation1nstd204human GRCh37.p13 chr1: 161,483,791-161,542,990 , GRCh38.p13 chr1: 161,514,001-161,573,200 FCGR2A, FCGR3A, 7 more genes
    nsv5214749copy number variation1nstd204human GRCh38.p13 chr1: 161,534,901-161,552,600 , GRCh37.p13 chr1: 161,504,691-161,522,390 FCGR3A, TRN-GTT1-1, 1 more genes
    nsv5212042copy number variation1nstd204human GRCh38.p13 chr1: 161,548,301-161,556,700 , GRCh37.p13 chr1: 161,518,091-161,526,490 FCGR3A
    nsv5209829copy number variation1nstd204human GRCh38.p13 chr1: 161,548,667-161,550,218 , GRCh37.p13 chr1: 161,518,457-161,520,008 FCGR3A
    nsv5209816copy number variation1nstd204human GRCh38.p13 chr1: 161,550,201-161,558,100 , GRCh37.p13 chr1: 161,519,991-161,527,890 FCGR3A
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