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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146743copy number variation1nstd232human GRCh37.p13 chr1: 109,314,929-109,314,983 , GRCh38.p12 chr1: 108,772,307-108,772,361 STXBP3
    nsv7141415copy number variation1nstd232human GRCh37.p13 chr1: 109,314,956-109,315,037 , GRCh38.p12 chr1: 108,772,334-108,772,415 STXBP3
    nsv7137790insertion1nstd232human GRCh37.p13 chr1: 109,313,979-109,313,979 , GRCh38.p12 chr1: 108,771,357-108,771,357 STXBP3
    nsv7099223copy number variation1nstd231human GRCh38.p12 chr1: 108,551,579-110,710,631 , GRCh37 chr1: 109,094,201-111,253,253 ALX3, AMPD2, 74 more genes
    nsv7095739copy number variation1nstd102humanPathogenic GRCh37 chr1: 108,679,275-111,674,176 , GRCh38.p12 chr1: 108,136,653-111,131,554 RPL7L1P21, GSTM4, 90 more genes
    nsv7095693copy number variation1nstd102humanUncertain significance GRCh37 chr1: 108,679,275-109,493,059 , GRCh38.p12 chr1: 108,136,653-108,950,437 AKNAD1, LOC105378890, 18 more genes
    nsv7048509inversion1nstd229human GRCh38 chr1: 108,319,829-109,244,823 , GRCh37.p13 chr1: 108,862,451-109,787,445 RPS27P6, ST13P21, 30 more genes
    nsv7044488inversion1nstd229human GRCh38 chr1: 100,052,919-109,025,639 , GRCh37.p13 chr1: 100,518,475-109,568,261 LOC102723784, DNAJA1P5, 109 more genes
    nsv6639723copy number variation1nstd229human GRCh38 chr1: 108,783,782-108,783,872 , GRCh37.p13 chr1: 109,326,404-109,326,494 STXBP3
    nsv6639722copy number variation1nstd229human GRCh38 chr1: 108,777,317-108,777,668 , GRCh37.p13 chr1: 109,319,939-109,320,290 STXBP3
    nsv6639721copy number variation1nstd229human GRCh38 chr1: 108,756,469-109,410,478 , GRCh37.p13 chr1: 109,299,091-109,953,100 PSMA5, STXBP3, 24 more genes
    nsv6639544copy number variation1nstd229human GRCh38 chr1: 108,800,946-108,805,751 , GRCh37.p13 chr1: 109,343,568-109,348,373 STXBP3
    nsv6639543copy number variation1nstd229human GRCh38 chr1: 108,780,593-109,355,741 , GRCh37.p13 chr1: 109,323,215-109,898,363 STXBP3, TMEM167B-DT, 22 more genes
    nsv6639542copy number variation1nstd229human GRCh38 chr1: 108,770,665-108,967,507 , GRCh37.p13 chr1: 109,313,287-109,510,129 SPATA42, LOC105378891, 4 more genes
    nsv6639541copy number variation1nstd229human GRCh38 chr1: 108,741,085-108,747,637 , GRCh37.p13 chr1: 109,283,707-109,290,259 FNDC7, STXBP3
    nsv6639411copy number variation1nstd229human GRCh38 chr1: 108,809,781-108,809,990 , GRCh37.p13 chr1: 109,352,403-109,352,612 STXBP3
    nsv6639410copy number variation1nstd229human GRCh38 chr1: 108,787,709-108,950,012 , GRCh37.p13 chr1: 109,330,331-109,492,634 STXBP3, AKNAD1, 4 more genes
    nsv6639409copy number variation1nstd229human GRCh38 chr1: 108,766,583-108,872,735 , GRCh37.p13 chr1: 109,309,205-109,415,357 LOC105378891, SPATA42, 3 more genes
    nsv6636972copy number variation1nstd102humanUncertain significance GRCh37 chr1: 109,345,620-109,404,928 , GRCh38.p12 chr1: 108,802,998-108,862,306 STXBP3, AKNAD1, 2 more genes
    nsv6636625copy number variation1nstd102humanUncertain significance GRCh37 chr1: 109,350,810-109,838,970 , GRCh38.p12 chr1: 108,808,188-109,296,348 CELSR2, RANP5, 21 more genes
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