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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143788copy number variation1nstd232human GRCh37.p13 chr3: 142,747,246-142,747,321 , GRCh38.p12 chr3: 143,028,404-143,028,479 U2SURP
    nsv7141510insertion1nstd232human GRCh37.p13 chr3: 142,720,515-142,720,515 , GRCh38.p12 chr3: 143,001,673-143,001,673 U2SURP, LOC100289361
    nsv6734899copy number variation1nstd229human GRCh38 chr3: 143,060,709-143,071,178 , GRCh37.p13 chr3: 142,779,551-142,790,020 U2SURP
    nsv6733710copy number variation1nstd229human GRCh38 chr3: 143,031,422-143,031,467 , GRCh37.p13 chr3: 142,750,264-142,750,309 U2SURP
    nsv6727008copy number variation1nstd229human GRCh38 chr3: 142,255,714-146,323,295 , GRCh37.p13 chr3: 141,974,556-146,041,082 LOC105374142, XRN1, 44 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6628696copy number variation1nstd224human GRCh37 chr3: 142,778,355-143,570,871 , GRCh38.p12 chr3: 143,059,513-143,852,029 PBX2P1, CHST2, 9 more genes
    nsv6567495inversion1nstd223human GRCh38 chr3: 143,008,761-143,009,612 , GRCh37.p13 chr3: 142,727,603-142,728,454 U2SURP
    nsv6562831inversion1nstd223human GRCh38 chr3: 142,555,219-148,451,915 , GRCh37.p13 chr3: 142,274,061-148,169,702 LOC102724145, PLS1, 60 more genes
    nsv6561353inversion1nstd223human GRCh38 chr3: 143,048,863-143,050,091 , GRCh37.p13 chr3: 142,767,705-142,768,933 U2SURP
    nsv6374149copy number variation1nstd223human GRCh38 chr3: 142,997,715-143,001,404 , GRCh37.p13 chr3: 142,716,557-142,720,246 U2SURP, LOC100289361, 1 more genes
    nsv6368929copy number variation1nstd223human GRCh38 chr3: 143,013,901-143,017,100 , GRCh37.p13 chr3: 142,732,743-142,735,942 U2SURP
    nsv6368773copy number variation1nstd223human GRCh38 chr3: 143,045,588-143,365,340 , GRCh37.p13 chr3: 142,764,430-143,084,182 CHST2, SLC9A9-AS1, 5 more genes
    nsv6364047copy number variation1nstd223human GRCh38 chr3: 142,868,501-143,010,800 , GRCh37.p13 chr3: 142,587,343-142,729,642 PCOLCE2, LOC100507389, 4 more genes
    nsv6363566copy number variation1nstd223human GRCh38 chr3: 143,036,275-143,036,842 , GRCh37.p13 chr3: 142,755,117-142,755,684 U2SURP
    nsv6362203copy number variation1nstd223human GRCh38 chr3: 143,025,736-143,026,269 , GRCh37.p13 chr3: 142,744,578-142,745,111 U2SURP
    nsv6359301copy number variation1nstd223human GRCh38 chr3: 143,055,015-143,055,445 , GRCh37.p13 chr3: 142,773,857-142,774,287 U2SURP
    nsv6308806mobile element insertion1nstd186human GRCh37 chr3: 142,747,741-142,747,792 , GRCh38.p12 chr3: 143,028,899-143,028,950 U2SURP
    nsv6290273copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,729,607-157,921,084 , GRCh38.p12 chr3: 143,010,765-158,203,295 LINC02066, TM4SF1-AS1, 206 more genes
    nsv6254775mobile element insertion1nstd215human GRCh38 chr3: 143,003,701-143,003,701 , GRCh37.p13 chr3: 142,722,543-142,722,543 U2SURP
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