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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112714copy number variation1nstd102humanPathogenic GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481 RNU6-789P, FAM86HP, 169 more genes
    nsv5889643copy number variation1nstd209human GRCh38 chr3: 130,044,537-130,087,901 , GRCh37.p13 chr3: 129,763,380-129,806,744 LINC02014, ALG1L2
    nsv5834901copy number variation1nstd209human GRCh38 chr3: 130,088,004-130,090,688 , GRCh37.p13 chr3: 129,806,847-129,809,531 ALG1L2, LINC02014
    nsv5834594copy number variation2nstd209human GRCh38 chr3: 130,084,615-130,088,353 , GRCh37.p13 chr3: 129,803,458-129,807,196 LINC02014, ALG1L2
    nsv5834311copy number variation2nstd209human GRCh38 chr3: 130,084,815-130,088,453 , GRCh37.p13 chr3: 129,803,658-129,807,296 ALG1L2, LINC02014
    nsv5623469insertion1nstd207human GRCh38 chr3: 130,090,879-130,090,879 , GRCh37.p13 chr3: 129,809,722-129,809,722 ALG1L2, LINC02014
    nsv5577656copy number variation1nstd207human GRCh38 chr3: 130,044,539-130,087,903 , GRCh37.p13 chr3: 129,763,382-129,806,746 LINC02014, ALG1L2
    nsv5569653copy number variation1nstd207human GRCh38 chr3: 130,085,209-130,087,616 , GRCh37.p13 chr3: 129,804,052-129,806,459 ALG1L2, LINC02014
    nsv5453311copy number variation1nstd206human GRCh38 chr3: 130,044,539-130,087,902 , GRCh37.p13 chr3: 129,763,382-129,806,745 ALG1L2, LINC02014
    nsv5317334copy number variation1nstd204human GRCh37.p13 chr3: 129,763,382-129,806,745 , GRCh38.p13 chr3: 130,044,539-130,087,902 ALG1L2, LINC02014
    nsv5238711copy number variation1nstd204human GRCh38.p13 chr3: 130,087,854-130,090,456 , GRCh37.p13 chr3: 129,806,697-129,809,299 ALG1L2, LINC02014
    nsv5237738copy number variation1nstd204human GRCh38.p13 chr3: 130,087,301-130,087,900 , GRCh37.p13 chr3: 129,806,144-129,806,743 ALG1L2, LINC02014
    nsv5236083copy number variation1nstd204human GRCh38.p13 chr3: 130,082,601-130,093,400 , GRCh37.p13 chr3: 129,801,444-129,812,243 LINC02014, ALG1L2
    nsv5235218copy number variation1nstd204human GRCh38.p13 chr3: 130,086,501-130,087,900 , GRCh37.p13 chr3: 129,805,344-129,806,743 LINC02014, ALG1L2
    nsv5233733copy number variation1nstd204human GRCh38.p13 chr3: 130,089,180-130,091,248 , GRCh37.p13 chr3: 129,808,023-129,810,091 LINC02014, ALG1L2
    nsv5233036copy number variation1nstd204human GRCh38.p13 chr3: 130,089,501-130,090,600 , GRCh37.p13 chr3: 129,808,344-129,809,443 LINC02014, ALG1L2
    nsv5232306copy number variation1nstd204human GRCh38.p13 chr3: 130,087,901-130,090,000 , GRCh37.p13 chr3: 129,806,744-129,808,843 ALG1L2, LINC02014
    nsv5231577copy number variation1nstd204human GRCh38.p13 chr3: 130,085,201-130,094,300 , GRCh37.p13 chr3: 129,804,044-129,813,143 ALG1L2, LINC02014
    nsv5229659copy number variation1nstd204human GRCh38.p13 chr3: 130,086,590-130,087,853 , GRCh37.p13 chr3: 129,805,433-129,806,696 LINC02014, ALG1L2
    nsv5229050copy number variation1nstd204human GRCh38.p13 chr3: 130,083,901-130,093,400 , GRCh37.p13 chr3: 129,802,744-129,812,243 ALG1L2, LINC02014
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