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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148271copy number variation1nstd102humanPathogenic GRCh38 chr18: 158,286-14,124,574 , GRCh37.p13 chr18: 158,286-14,124,573 PMM2P2, EIF4A2P1, 225 more genes
    nsv7098917copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-15,400,035 , GRCh38.p12 chr18: 10,001-15,400,036 RNU7-25P, RPL6P27, 275 more genes
    nsv7094930copy number variation1nstd102humanUncertain significance GRCh37 chr18: 2,656,075-3,457,938 , GRCh38.p12 chr18: 2,656,076-3,457,940 EMILIN2, RNU7-25P, 16 more genes
    nsv7014657copy number variation1nstd229human GRCh38 chr18: 3,430,301-3,443,900 , GRCh37.p13 chr18: 3,430,299-3,443,898 TGIF1
    nsv7014486copy number variation1nstd229human GRCh38 chr18: 3,393,401-3,715,600 , GRCh37.p13 chr18: 3,393,399-3,715,600 LOC105371967, GAPLINC, 10 more genes
    nsv7011531copy number variation1nstd229human GRCh38 chr18: 3,435,041-3,438,985 , GRCh37.p13 chr18: 3,435,039-3,438,983 TGIF1
    nsv7006434copy number variation1nstd229human GRCh38 chr18: 3,429,499-3,435,927 , GRCh37.p13 chr18: 3,429,497-3,435,925 TGIF1
    nsv7006371copy number variation1nstd229human GRCh38 chr18: 3,430,557-3,434,477 , GRCh37.p13 chr18: 3,430,555-3,434,475 TGIF1
    nsv7004187copy number variation1nstd229human GRCh38 chr18: 3,414,743-3,414,968 , GRCh37.p13 chr18: 3,414,741-3,414,966 TGIF1, BOD1P1
    nsv7000847copy number variation1nstd229human GRCh38 chr18: 3,415,823-3,419,757 , GRCh37.p13 chr18: 3,415,821-3,419,755 BOD1P1, TGIF1
    nsv6637684copy number variation1nstd102humanUncertain significance GRCh37 chr18: 2,818,532-3,412,231 , GRCh38.p12 chr18: 2,818,534-3,412,233 RPL31P59, IGLJCOR18, 14 more genes
    nsv6637665copy number variation1nstd102humanPathogenic GRCh37 chr18: 2,255,007-4,488,934 , GRCh38.p12 chr18: 2,255,007-4,488,934 DLGAP1-AS4, MYL12-AS1, 38 more genes
    nsv6637580copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-7,218,594 , GRCh38.p12 chr18: 136,227-7,218,596 L3MBTL4-AS1, LOC101927044, 106 more genes
    nsv6637521copy number variation1nstd102humanUncertain significance GRCh37 chr18: 2,485,817-4,086,341 , GRCh38.p12 chr18: 2,485,818-4,086,341 DLGAP1-AS4, EMILIN2, 35 more genes
    nsv6637285copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-11,283,184 , GRCh38.p12 chr18: 136,227-11,283,185 EMILIN2, KRT18P8, 165 more genes
    nsv6634418copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-8,638,260 , GRCh38.p12 chr18: 10,001-8,638,262 AKAIN1, LPIN2, 126 more genes
    nsv6624589copy number variation1nstd224human GRCh37 chr18: 3,414,008-3,729,292 , GRCh38.p12 chr18: 3,414,010-3,729,292 LOC100419892, TGIF1, 8 more genes
    nsv6624552copy number variation1nstd224human GRCh37 chr18: 3,362,029-3,424,358 , GRCh38.p12 chr18: 3,362,031-3,424,360 TGIF1, BOD1P1, 3 more genes
    nsv6595231inversion1nstd223human GRCh38 chr18: 3,427,885-3,428,458 , GRCh37.p13 chr18: 3,427,883-3,428,456 TGIF1
    nsv6591773inversion1nstd223human GRCh38 chr18: 3,429,967-3,430,663 , GRCh37.p13 chr18: 3,429,965-3,430,661 TGIF1
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