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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095726copy number variation1nstd102humanPathogenic GRCh37 chr19: 6,361,586-8,212,364 , GRCh38.p12 chr19: 6,361,575-8,147,480 SLC25A23, LYPLA2P2, 77 more genes
    nsv7095676copy number variation1nstd102humanUncertain significance GRCh37 chr19: 7,586,521-8,670,595 , GRCh38.p12 chr19: 7,521,635-8,605,710 LRRC8E, ZNF414, 53 more genes
    nsv7070187inversion1nstd229human GRCh38 chr19: 6,518,823-8,315,881 , GRCh37.p13 chr19: 6,518,834-8,380,765 , ZNF557, 69 more genes
    nsv7066716inversion1nstd229human GRCh38 chr19: 6,518,017-8,344,162 , GRCh37.p13 chr19: 6,518,028-8,409,046 , STXBP2, 71 more genes
    nsv7062847inversion1nstd229human GRCh38 chr19: 7,473,530-8,349,302 , GRCh37.p13 chr19: 7,538,416-8,414,186 CERS4, LYPLA2P2, 47 more genes
    nsv7058385inversion1nstd229human GRCh38 chr19: 7,791,153-7,795,115 , GRCh37.p13 chr19: 7,856,039-7,860,001 CLEC4GP1
    nsv7016325copy number variation1nstd229human GRCh38 chr19: 7,782,901-7,790,900 , GRCh37.p13 chr19: 7,847,787-7,855,786 CLEC4GP1, LOC105372263
    nsv7013524copy number variation1nstd229human GRCh38 chr19: 7,623,595-7,921,993 , GRCh37.p13 chr19: 7,688,481-7,986,878 STXBP2, LOC100129391, 24 more genes
    nsv7012626copy number variation1nstd229human GRCh38 chr19: 7,778,106-7,791,068 , GRCh37.p13 chr19: 7,842,992-7,855,954 CLEC4GP1, LOC105372263
    nsv7011964copy number variation1nstd229human GRCh38 chr19: 7,354,369-9,019,195 , GRCh37.p13 chr19: 7,419,271-9,129,871 , MCOLN1, 66 more genes
    nsv7011121copy number variation1nstd229human GRCh38 chr19: 7,159,006-9,938,147 , GRCh37.p13 chr19: 7,159,017-10,048,823 , OR7G1, 117 more genes
    nsv7006012copy number variation1nstd229human GRCh38 chr19: 7,766,114-7,797,343 , GRCh37.p13 chr19: 7,831,000-7,862,229 CLEC4GP1, CLEC4M, 1 more genes
    nsv6625513copy number variation1nstd224human GRCh37 chr19: 7,761,802-7,872,768 , GRCh38.p12 chr19: 7,696,916-7,807,882 FCER2, CLEC4M, 7 more genes
    nsv6625331copy number variation1nstd224human GRCh37 chr19: 7,663,768-7,881,030 , GRCh38.p12 chr19: 7,598,882-7,816,144 FCER2, STXBP2, 18 more genes
    nsv6532645copy number variation1nstd223human GRCh38 chr19: 7,768,415-7,825,056 , GRCh37.p13 chr19: 7,833,301-7,889,942 CLEC4GP1, CLEC4M, 2 more genes
    nsv6523679copy number variation1nstd223human GRCh38 chr19: 7,778,105-7,791,072 , GRCh37.p13 chr19: 7,842,991-7,855,958 CLEC4GP1, LOC105372263
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133528copy number variation1nstd213human GRCh37 chr19: 7,780,000-8,030,001 , GRCh38.p12 chr19: 7,715,114-7,965,117 TIMM44, PRR36, 17 more genes
    nsv6133479copy number variation1nstd213human GRCh37 chr19: 7,400,000-13,280,001 , GRCh38.p12 chr19: 7,335,095-13,169,187 , ACP5, 299 more genes
    nsv5175447mobile element insertion1nstd203human GRCh38 chr19: 7,785,738-7,785,750 , GRCh37.p13 chr19: 7,850,624-7,850,636 LOC105372263, CLEC4GP1
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