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Items: 9

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    Number of Variants: 9

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6313574copy number variation1nstd102humanPathogenic GRCh37 chr1: 68,180,293-92,731,957 , GRCh38.p12 chr1: 67,714,610-92,266,400 GBP6, RNA5SP51, 315 more genes
    nsv3885743copy number variation1nstd102humanPathogenic GRCh37 chr1: 72,044,544-92,505,091 , GRCh38.p12 chr1: 71,578,861-92,039,534 GBP6, ZNHIT6, 257 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 GBP6, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 GBP6, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 GBP6, 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 GBP6, LINC01773, 322 more genes
    nsv3908786copy number variation1nstd102humanLikely benign NCBI36 chr1: 89,432,262-89,718,678 , GRCh37 chr1: 89,659,674-89,946,090 , GRCh38 chr1: 89,193,991-89,480,531 GBP6, GBP4, 7 more genes
    nsv4451609copy number variation1nstd102humanUncertain significance GRCh37 chr1: 89,546,802-90,520,362 , GRCh38.p12 chr1: 89,081,119-90,054,804 GBP6, 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 GBP6, LINC01776, 1853 more genes
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