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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112736copy number variation1nstd102humanPathogenic GRCh37 chr10: 48,301,535-51,807,296 , GRCh38.p12 chr10: 45,999,930-49,959,916 SHLD2P3, LOC100420617, 95 more genes
    nsv5963865insertion1nstd209human GRCh38 chr10: 48,181,878-48,181,878 , GRCh37.p13 chr10: 49,389,921-49,389,921 FRMPD2
    nsv5948358insertion1nstd209human GRCh38 chr10: 48,183,851-48,183,851 , GRCh37.p13 chr10: 49,391,894-49,391,894 FRMPD2
    nsv5927527copy number variation1nstd209human GRCh38 chr10: 48,188,701-48,189,497 , GRCh37.p13 chr10: 49,396,744-49,397,540 FRMPD2
    nsv5916113copy number variation1nstd209human GRCh38 chr10: 45,791,488-50,132,032 , GRCh37.p13 chr10|NW_003871068.1: 62,603-2,281,126 , GRCh37.p13 chr10: 46,591,857-51,891,792 , LINC02675, 111 more genes
    nsv5914502copy number variation1nstd209human GRCh38 chr10: 45,768,833-50,109,449 , GRCh37.p13 chr10: 46,591,857-51,028,871 , GRCh37.p13 chr10|NW_003871068.1: 39,948-2,281,126 , AGAP13P, 111 more genes
    nsv5912885copy number variation1nstd209human GRCh38 chr10: 48,189,737-48,189,797 , GRCh37.p13 chr10: 49,397,780-49,397,840 FRMPD2
    nsv5908714copy number variation1nstd209human GRCh38 chr10: 48,249,809-48,249,874 , GRCh37.p13 chr10: 49,457,852-49,457,917 FRMPD2
    nsv5865796copy number variation1nstd209human GRCh38 chr10: 48,171,657-48,178,498 , GRCh37.p13 chr10: 46,672,248-46,679,092 FRMPD2
    nsv5862536copy number variation1nstd209human GRCh38 chr10: 48,174,711-48,187,810 , GRCh37.p13 chr10: 49,382,754-49,389,702 FRMPD2
    nsv5851046copy number variation1nstd209human GRCh38 chr10: 48,249,649-48,251,648 , GRCh37.p13 chr10: 49,457,692-49,459,691 FRMPD2
    nsv5849712copy number variation1nstd209human GRCh38 chr10: 48,248,849-48,251,198 , GRCh37.p13 chr10: 49,456,892-49,459,241 FRMPD2
    nsv5849191copy number variation1nstd209human GRCh38 chr10: 48,235,821-48,269,449 , GRCh37.p13 chr10: 49,443,864-49,477,492 FRMPD2
    nsv5704954mobile element insertion1nstd211human GRCh38 chr10: 48,221,055-48,221,055 , GRCh37.p13 chr10: 49,429,098-49,429,098 FRMPD2
    nsv5585390copy number variation1nstd207human GRCh38 chr10: 48,249,809-48,249,874 , GRCh37.p13 chr10: 49,457,852-49,457,917 FRMPD2
    nsv5554295sequence alteration1nstd206human GRCh38 chr10: 48,251,776-48,281,663 , GRCh37.p13 chr10: 49,459,819-49,489,706 FRMPD2
    nsv5485525copy number variation1nstd206human GRCh38 chr10: 48,199,313-48,199,404 , GRCh37.p13 chr10: 49,407,356-49,407,447 FRMPD2
    nsv5483530copy number variation1nstd206human GRCh38 chr10: 48,085,184-48,168,634 , GRCh37.p13 chr10: 46,591,857-46,669,220 PTPN20CP, FRMPD2
    nsv5483515copy number variation1nstd206human GRCh38 chr10: 47,586,000-50,754,368 , GRCh37.p13 chr10: 46,591,857-52,514,128 HMGB1P50, PARG, 65 more genes
    nsv5481738copy number variation1nstd206human GRCh38 chr10: 48,154,234-48,164,559 , GRCh37.p13 chr10: 46,654,811-46,665,141 FRMPD2
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