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    Number of Variants: 10

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3883711copy number variation1nstd102humanBenign GRCh37 chr1: 90,022,057-90,022,796 , GRCh38.p12 chr1: 89,556,498-89,557,237 LRRC8B
    nsv6313574copy number variation1nstd102humanPathogenic GRCh37 chr1: 68,180,293-92,731,957 , GRCh38.p12 chr1: 67,714,610-92,266,400 LRRC8B, RNA5SP51, 315 more genes
    nsv3885743copy number variation1nstd102humanPathogenic GRCh37 chr1: 72,044,544-92,505,091 , GRCh38.p12 chr1: 71,578,861-92,039,534 LRRC8B, ZNHIT6, 257 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 LRRC8B, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 LRRC8B, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 LRRC8B, RNU1-153P, 4887 more genes
    nsv3898327copy number variation1nstd102humanPathogenic GRCh38 chr1: 83,457,325-104,273,917 , GRCh37 chr1: 83,923,008-104,816,539 , NCBI36 chr1: 83,695,596-104,618,062 LRRC8B, LINC01773, 322 more genes
    nsv3876714copy number variation1nstd102humanLikely benign GRCh37 chr1: 89,898,842-90,679,734 , GRCh38.p12 chr1: 89,433,283-90,214,176 LRRC8B, LOC100505788, 12 more genes
    nsv4451609copy number variation1nstd102humanUncertain significance GRCh37 chr1: 89,546,802-90,520,362 , GRCh38.p12 chr1: 89,081,119-90,054,804 LRRC8B, GBP2, 25 more genes
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 LRRC8B, LINC01776, 1853 more genes
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