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Items: 1 to 20 of 838

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6115724mobile element insertion1nstd186human GRCh37 chr22: 22,376,447-22,376,498 , GRCh38.p12 chr22: 22,022,049-22,022,100 PRAMENP
    nsv5970269insertion1nstd209human GRCh38 chr22: 22,022,033-22,022,033 , GRCh37.p13 chr22: 22,376,431-22,376,431 PRAMENP
    nsv5966353copy number variation1nstd209human GRCh38 chr22: 22,019,691-22,019,740 , GRCh37.p13 chr22: 22,374,089-22,374,138 PRAMENP
    nsv5959252copy number variation1nstd209human GRCh38 chr22: 22,031,472-22,168,098 , GRCh37.p13 chr22: 22,385,870-22,522,491 IGLVI-68, IGLV4-69, 15 more genes
    nsv5959042copy number variation1nstd209human GRCh38 chr22: 22,026,551-22,904,986 , GRCh37.p13 chr22: 22,380,949-23,247,166 , IGLV1-44, 113 more genes
    nsv5957865copy number variation1nstd209human GRCh38 chr22: 22,031,459-22,893,783 , GRCh37.p13 chr22: 22,385,857-23,235,963 , IGLV7-46, 108 more genes
    nsv5955655copy number variation1nstd209human GRCh38 chr22: 22,019,005-22,025,039 , GRCh37.p13 chr22: 22,373,403-22,379,437 IGL, IGLVI-70, 1 more genes
    nsv5953877copy number variation1nstd209human GRCh38 chr22: 22,031,467-22,899,623 , GRCh37.p13 chr22: 22,385,865-23,241,803 , LOC100419915, 110 more genes
    nsv5952603copy number variation1nstd209human GRCh38 chr22: 22,026,550-22,899,617 , GRCh37.p13 chr22: 22,380,948-23,241,797 , VPREB1, 111 more genes
    nsv5949766copy number variation1nstd209human GRCh38 chr22: 22,026,550-22,893,779 , GRCh37.p13 chr22: 22,380,948-23,235,959 , IGLV2-5, 109 more genes
    nsv5947607copy number variation1nstd209human GRCh38 chr22: 22,031,465-22,904,986 , GRCh37.p13 chr22: 22,385,863-23,247,166 , IGLV3-15, 112 more genes
    nsv5884168copy number variation2nstd209human GRCh38 chr22: 22,026,545-22,033,440 , GRCh37.p13 chr22: 22,380,943-22,387,838 IGLVI-68, PRAMENP, 3 more genes
    nsv5883271copy number variation2nstd209human GRCh38 chr22: 22,039,541-22,049,777 , GRCh37.p13 chr22: 22,393,940-22,404,175 IGL, IGLV10-67, 1 more genes
    nsv5883263copy number variation1nstd209human GRCh38 chr22: 21,956,717-22,015,267 , GRCh37.p13 chr22: 22,311,089-22,369,665 TOP3B, PRAMENP
    nsv5882224copy number variation2nstd209human GRCh38 chr22: 22,030,016-22,042,040 , GRCh37.p13 chr22: 22,384,414-22,396,438 IGL, IGLVI-68, 3 more genes
    nsv5881744copy number variation2nstd209human GRCh38 chr22: 22,032,341-22,042,623 , GRCh37.p13 chr22: 22,386,739-22,397,021 IGLVI-68, IGLV10-67, 2 more genes
    nsv5880142copy number variation2nstd209human GRCh38 chr22: 22,030,316-22,033,440 , GRCh37.p13 chr22: 22,384,714-22,387,838 IGLVI-68, PRAMENP, 2 more genes
    nsv5874360copy number variation2nstd209human GRCh38 chr22: 22,026,520-22,037,365 , GRCh37.p13 chr22: 22,380,918-22,391,764 IGLVI-68, IGLVI-70, 3 more genes
    nsv5873216copy number variation1nstd209human GRCh38 chr22: 22,013,318-22,020,617 , GRCh37.p13 chr22: 22,367,716-22,375,015 PRAMENP
    nsv5872468copy number variation2nstd209human GRCh38 chr22: 22,029,516-22,034,940 , GRCh37.p13 chr22: 22,383,914-22,389,339 IGLVI-68, IGLV4-69, 2 more genes
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