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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098718copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,206,913-3,771,740 , GRCh38.p12 chr19: 1,206,914-3,771,742 GIPC3, GNG7, 117 more genes
    nsv7095644copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,456,055-2,456,931 , GRCh38.p12 chr19: 1,456,056-2,456,933 APC2, CSNK1G2, 49 more genes
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 NCLN, RN7SL202P, 223 more genes
    nsv7095296copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-2,151,333 , GRCh38.p12 chr19: 589,946-2,151,334 ADAMTSL5, GPX4, 90 more genes
    nsv7095269copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,465,134-1,497,210 , GRCh38.p12 chr19: 1,465,135-1,497,211 C19orf25, APC2, 2 more genes
    nsv7095264copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,206,913-1,650,247 , GRCh38.p12 chr19: 1,206,914-1,650,248 NDUFS7, GAMT, 30 more genes
    nsv7095226copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-4,818,389 , GRCh38.p12 chr19: 589,946-4,818,377 ATP5F1D, LOC102723798, 204 more genes
    nsv7095190copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,455,264-1,455,852 , GRCh38.p12 chr19: 1,455,265-1,455,853 APC2
    nsv7070296inversion1nstd229human GRCh38 chr19: 1,461,618-2,158,584 , GRCh37.p13 chr19: 1,461,617-2,158,583 BTBD2, MEX3D, 30 more genes
    nsv7016666copy number variation1nstd229human GRCh38 chr19: 1,441,938-1,462,680 , GRCh37.p13 chr19: 1,441,937-1,462,679 APC2
    nsv7013976copy number variation1nstd229human GRCh38 chr19: 1,440,873-1,444,938 , GRCh37.p13 chr19: 1,440,872-1,444,937 APC2, RPS15
    nsv7006261copy number variation1nstd229human GRCh38 chr19: 1,420,401-1,679,000 , GRCh37.p13 chr19: 1,420,400-1,678,999 C19orf25, PLK5, 13 more genes
    nsv7004389copy number variation1nstd229human GRCh38 chr19: 1,468,501-1,471,600 , GRCh37.p13 chr19: 1,468,500-1,471,599 APC2, C19orf25
    nsv7003742copy number variation1nstd229human GRCh38 chr19: 1,442,340-1,448,219 , GRCh37.p13 chr19: 1,442,339-1,448,218 APC2
    nsv7002911copy number variation1nstd229human GRCh38 chr19: 1,460,090-1,510,967 , GRCh37.p13 chr19: 1,460,089-1,510,966 C19orf25, ADAMTSL5, 3 more genes
    nsv7001918copy number variation1nstd229human GRCh38 chr19: 1,460,301-1,487,100 , GRCh37.p13 chr19: 1,460,300-1,487,099 PCSK4, C19orf25, 1 more genes
    nsv6637582copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,356,893-1,676,446 , GRCh38.p12 chr19: 1,356,894-1,676,447 REEP6, GAMT, 18 more genes
    nsv6637184copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,205,244-1,479,188 , GRCh38.p12 chr19: 1,205,245-1,479,189 C19orf25, EFNA2, 19 more genes
    nsv6624832copy number variation1nstd224human GRCh37 chr19: 1,462,052-1,483,428 , GRCh38.p12 chr19: 1,462,053-1,483,429 APC2, PCSK4, 1 more genes
    nsv6624831copy number variation1nstd224human GRCh37 chr19: 1,462,052-1,483,326 , GRCh38.p12 chr19: 1,462,053-1,483,327 APC2, PCSK4, 1 more genes
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