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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
    nsv7095258copy number variation1nstd102humanUncertain significance GRCh37 chr18: 9,102,742-12,725,530 , GRCh38.p12 chr18: 9,102,744-12,725,531 PIEZO2, RALBP1, 77 more genes
    nsv7076310inversion1nstd229human GRCh38 chr18: 7,168,687-9,983,107 , GRCh37.p13 chr18: 7,168,686-9,983,104 MTCL1, LOC112577592, 40 more genes
    nsv7075855inversion1nstd229human GRCh38 chr18: 6,609,506-9,295,232 , GRCh37.p13 chr18: 6,609,505-9,295,230 LAMA1, RAB12, 28 more genes
    nsv7074186inversion1nstd229human GRCh38 chr18: 7,953,048-15,343,982 , GRCh37.p13 chr18: 7,953,046-15,343,981 PSMG2, EIF4A2P1, 155 more genes
    nsv7065817inversion1nstd229human GRCh38 chr18: 6,839,495-9,543,414 , GRCh37.p13 chr18: 6,839,494-9,543,412 ANKRD12, RPS4XP19, 32 more genes
    nsv7016649copy number variation1nstd229human GRCh38 chr18: 9,076,136-9,124,009 , GRCh37.p13 chr18: 9,076,134-9,124,007 NDUFV2-AS1, NDUFV2
    nsv7015597copy number variation1nstd229human GRCh38 chr18: 9,101,118-9,101,249 , GRCh37.p13 chr18: 9,101,116-9,101,247 NDUFV2
    nsv7015128copy number variation1nstd229human GRCh38 chr18: 4,434,377-14,413,632 , GRCh37.p13 chr18: 4,434,377-14,413,631 RAB31, THEMIS3P, 167 more genes
    nsv7011343copy number variation1nstd229human GRCh38 chr18: 9,111,766-9,116,700 , GRCh37.p13 chr18: 9,111,764-9,116,698 NDUFV2
    nsv7010345copy number variation1nstd229human GRCh38 chr18: 9,116,046-9,163,839 , GRCh37.p13 chr18: 9,116,044-9,163,837 NDUFV2, NDUFV2-AS1, 1 more genes
    nsv7008176copy number variation1nstd229human GRCh38 chr18: 9,103,896-9,105,709 , GRCh37.p13 chr18: 9,103,894-9,105,707 NDUFV2
    nsv7007757copy number variation1nstd229human GRCh38 chr18: 9,101,910-9,103,314 , GRCh37.p13 chr18: 9,101,908-9,103,312 NDUFV2
    nsv7005547copy number variation1nstd229human GRCh38 chr18: 9,111,513-9,112,104 , GRCh37.p13 chr18: 9,111,511-9,112,102 NDUFV2
    nsv7003227copy number variation1nstd229human GRCh38 chr18: 9,101,818-9,111,769 , GRCh37.p13 chr18: 9,101,816-9,111,767 NDUFV2
    nsv6998909copy number variation1nstd229human GRCh38 chr18: 9,122,275-9,122,302 , GRCh37.p13 chr18: 9,122,273-9,122,300 NDUFV2-AS1, NDUFV2
    nsv6998606copy number variation1nstd229human GRCh38 chr18: 9,096,956-9,110,296 , GRCh37.p13 chr18: 9,096,954-9,110,294 NDUFV2
    nsv6637624copy number variation1nstd102humanUncertain significance GRCh37 chr18: 8,585,096-9,660,466 , GRCh38.p12 chr18: 8,585,098-9,660,468 TWSG1-DT, RPS4XP19, 16 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
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