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    Number of Variants: 10

    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 CDC7, RNA5SP51, 315 more genes
    nsv3885743copy number variation1nstd102humanPathogenic GRCh37 chr1: 72,044,544-92,505,091 , GRCh38.p12 chr1: 71,578,861-92,039,534 CDC7, ZNHIT6, 257 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 CDC7, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 CDC7, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 CDC7, 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 CDC7, LINC01773, 322 more genes
    nsv3882533copy number variation1nstd102humanBenign GRCh37 chr1: 91,690,179-92,082,962 , GRCh38.p12 chr1: 91,224,622-91,617,405 CDC7, FEN1P1, 6 more genes
    nsv4728136copy number variation1nstd102humanUncertain significance GRCh37 chr1: 91,626,271-92,080,577 , GRCh38.p12 chr1: 91,160,714-91,615,020 CDC7, LOC105378856, 6 more genes
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 CDC7, LINC01776, 1853 more genes
    nsv3873752copy number variation1nstd102humanUncertain significance GRCh37 chr1: 91,668,330-93,539,185 , GRCh38.p12 chr1: 91,202,773-93,073,628 CDC7, RNU4-59P, 38 more genes
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