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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148175copy number variation1nstd102humanPathogenic GRCh38 chr1: 230,178,121-243,646,135 , GRCh37.p13 chr1: 230,313,867-243,809,437 AGT, MAP10, 221 more genes
    nsv7148158copy number variation1nstd102humanPathogenic GRCh38 chr1: 235,215,476-247,005,888 , GRCh37.p13 chr1: 235,378,791-247,169,190 RNU6-747P, LINC01139, 172 more genes
    nsv7099270copy number variation1nstd231human GRCh38.p12 chr1: 237,610,040-242,246,069 , GRCh37 chr1: 237,773,340-242,409,371 CHML, CHRM3, 59 more genes
    nsv7095520copy number variation1nstd102humanUncertain significance GRCh37 chr1: 241,661,128-244,218,672 , GRCh38.p12 chr1: 241,497,828-244,055,370 LOC105373231, LOC105373234, 39 more genes
    nsv7093371copy number variation1nstd102humannot provided GRCh37 chr1: 224,230,307-243,181,599 , GRCh38.p12 chr1: 224,042,605-243,018,297 RPL36P6, MTND4LP21, 377 more genes
    nsv7050815inversion1nstd229human GRCh38 chr1: 240,664,933-241,655,110 , GRCh37.p13 chr1: 240,828,233-241,818,412 THAP12P8, OPN3, 12 more genes
    nsv7048087inversion1nstd229human GRCh38 chr1: 240,132,685-242,030,818 , GRCh37.p13 chr1: 240,295,985-242,194,120 RPS11P2, MIR3123, 27 more genes
    nsv7040493inversion1nstd229human GRCh38 chr1: 240,436,239-242,512,823 , GRCh37.p13 chr1: 240,599,539-242,676,125 CFL1P4, RNU5F-8P, 34 more genes
    nsv7038410inversion1nstd229human GRCh38 chr1: 240,665,018-241,655,164 , GRCh37.p13 chr1: 240,828,318-241,818,466 LOC100506929, MIR3123, 12 more genes
    nsv6675734copy number variation1nstd229human GRCh38 chr1: 241,606,663-241,626,636 , GRCh37.p13 chr1: 241,769,965-241,789,938 OPN3
    nsv6673142copy number variation1nstd229human GRCh38 chr1: 240,779,703-242,915,971 , GRCh37.p13 chr1: 240,943,003-243,079,273 OPN3, LOC107985466, 30 more genes
    nsv6672742copy number variation1nstd229human GRCh38 chr1: 241,326,784-241,678,502 , GRCh37.p13 chr1: 241,490,084-241,841,804 KMO, RGS7, 4 more genes
    nsv6669542copy number variation1nstd229human GRCh38 chr1: 241,614,814-241,616,802 , GRCh37.p13 chr1: 241,778,116-241,780,104 OPN3
    nsv6665585copy number variation1nstd229human GRCh38 chr1: 241,599,419-241,602,629 , GRCh37.p13 chr1: 241,762,721-241,765,931 OPN3
    nsv6663982copy number variation1nstd229human GRCh38 chr1: 240,912,743-242,394,973 , GRCh37.p13 chr1: 241,076,043-242,558,275 HNRNPA1P42, LOC105373231, 24 more genes
    nsv6663839copy number variation1nstd229human GRCh38 chr1: 241,620,051-241,632,340 , GRCh37.p13 chr1: 241,783,353-241,795,642 CHML, OPN3
    nsv6661776copy number variation1nstd229human GRCh38 chr1: 241,616,536-241,628,346 , GRCh37.p13 chr1: 241,779,838-241,791,648 CHML, OPN3
    nsv6661680copy number variation1nstd229human GRCh38 chr1: 241,326,577-241,683,439 , GRCh37.p13 chr1: 241,489,877-241,846,741 WDR64, OPN3, 4 more genes
    nsv6661331copy number variation1nstd229human GRCh38 chr1: 241,623,052-241,625,986 , GRCh37.p13 chr1: 241,786,354-241,789,288 OPN3
    nsv6659152copy number variation1nstd229human GRCh38 chr1: 241,640,202-241,640,809 , GRCh37.p13 chr1: 241,803,504-241,804,111 OPN3
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