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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3876712copy number variation1nstd102humanBenign GRCh37 chr1: 210,712,495-210,724,717 , GRCh38.p12 chr1|NW_011332687.1: 318,893-331,115 , GRCh38.p12 chr1: 210,539,151-210,551,373 HHAT
    nsv3882268copy number variation1nstd102humanBenign GRCh37 chr1: 210,722,554-210,726,823 , GRCh38.p12 chr1: 210,549,210-210,553,479 , GRCh38.p12 chr1|NW_011332687.1: 328,952-333,221 HHAT
    nsv3877373copy number variation1nstd102humanBenign GRCh37 chr1: 210,721,874-210,724,779 , GRCh38.p12 chr1: 210,548,530-210,551,435 , GRCh38.p12 chr1|NW_011332687.1: 328,272-331,177 HHAT
    nsv3885535copy number variation1nstd102humanBenign GRCh37 chr1: 210,722,554-210,724,779 , GRCh38.p12 chr1|NW_011332687.1: 328,952-331,177 , GRCh38.p12 chr1: 210,549,210-210,551,435 HHAT
    nsv3882972copy number variation1nstd102humanBenign GRCh37 chr1: 210,722,554-210,724,717 , GRCh38.p12 chr1: 210,549,210-210,551,373 , GRCh38.p12 chr1|NW_011332687.1: 328,952-331,115 HHAT
    nsv6313883copy number variation1nstd102humanUncertain significance GRCh37 chr1: 210,786,742-210,858,579 , GRCh38.p12 chr1: 210,613,398-210,685,237 , GRCh38.p12 chr1|NW_011332687.1: 393,140-460,100 HHAT, KCNH1
    nsv4452102copy number variation1nstd102humanUncertain significance GRCh37 chr1: 210,763,715-210,951,892 , GRCh38.p12 chr1: 210,590,371-210,778,550 HHAT, LOC105372901, 1 more genes
    nsv3881313copy number variation1nstd102humanPathogenic GRCh37 chr1: 204,682,513-212,815,646 , GRCh38.p12 chr1: 204,713,385-212,642,304 HHAT, IL19, 184 more genes
    nsv3917200copy number variation1nstd102humanPathogenic NCBI36 chr1: 206,303,429-210,147,777 , GRCh37.p13 chr1: 208,236,806-212,081,154 , GRCh38.p12 chr1: 208,063,461-211,907,812 HHAT, LOC105372904, 68 more genes
    nsv3870695copy number variation1nstd102humanPathogenic GRCh37 chr1: 209,742,722-210,774,573 , GRCh38.p12 chr1: 209,569,377-210,601,229 HHAT, RNASEH1P3, 19 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 HHAT, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 HHAT, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 HHAT, RNU1-153P, 4887 more genes
    nsv4450583copy number variation1nstd102humanPathogenic GRCh37 chr1: 182,388,773-249,111,240 , GRCh38.p12 chr1: 182,419,638-248,817,041 HHAT, RGS18, 1186 more genes
    nsv3881012copy number variation1nstd102humanPathogenic GRCh37 chr1: 195,483,439-249,213,000 , GRCh38.p12 chr1: 195,514,309-248,918,801 HHAT, LOC105372928, 1062 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 HHAT, LOC105373279, 1036 more genes
    nsv4674140copy number variation1nstd102humanPathogenic GRCh37 chr1: 204,045,948-249,218,992 , GRCh38.p12 chr1: 204,076,820-248,924,793 HHAT, RNA5S8, 893 more genes
    nsv3897747copy number variation1nstd102humanPathogenic GRCh38 chr1: 207,346,642-248,930,485 , GRCh37 chr1: 207,519,987-249,224,684 , NCBI36 chr1: 205,586,610-247,191,307 HHAT, RPS18P3, 793 more genes
    nsv3890682copy number variation1nstd102humanPathogenic GRCh37 chr1: 209,819,552-249,225,312 , NCBI36 chr1: 207,886,175-247,191,935 , GRCh38 chr1: 209,646,207-248,931,113 HHAT, HLX, 749 more genes
    nsv3892818copy number variation1nstd102humanPathogenic GRCh38 chr1: 209,963,625-248,918,469 , GRCh37 chr1: 210,136,970-249,212,668 , NCBI36 chr1: 208,203,593-247,179,291 HHAT, LOC105373046, 740 more genes
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