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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096096copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr21: 43,160,998-47,754,702 , GRCh38.p12 chr21: 41,740,838-46,334,788 TSPEAR, LINC01424, 158 more genes
    nsv7076050inversion1nstd229human GRCh38 chr21: 45,605,764-46,186,956 , GRCh37.p13 chr21: 47,025,678-47,606,870 SPATC1L, PCBP3, 11 more genes
    nsv7075824inversion1nstd229human GRCh38 chr21: 46,168,916-46,168,954 , GRCh37.p13 chr21: 47,588,830-47,588,868 SPATC1L
    nsv7065977inversion1nstd229human GRCh38 chr21: 46,100,911-46,189,866 , GRCh37.p13 chr21: 47,520,825-47,609,780 LSS, COL6A2, 3 more genes
    nsv7037973copy number variation1nstd229human GRCh38 chr21: 46,121,114-46,351,190 , GRCh37.p13 chr21: 47,541,028-47,771,104 C21orf58, PCNT, 9 more genes
    nsv7037855copy number variation1nstd229human GRCh38 chr21: 46,184,781-46,216,755 , GRCh37.p13 chr21: 47,604,695-47,636,669 LSS, SPATC1L, 1 more genes
    nsv7036785copy number variation1nstd229human GRCh38 chr21: 46,056,327-46,224,819 , GRCh37.p13 chr21: 47,476,241-47,644,733 FTCD, PSMA6P3, 5 more genes
    nsv7034788copy number variation1nstd229human GRCh38 chr21: 46,158,156-46,161,432 , GRCh37.p13 chr21: 47,578,070-47,581,346 SPATC1L
    nsv7034249copy number variation1nstd229human GRCh38 chr21: 46,125,401-46,161,300 , GRCh37.p13 chr21: 47,545,315-47,581,214 SPATC1L, COL6A2, 2 more genes
    nsv7033216copy number variation1nstd229human GRCh38 chr21: 46,172,090-46,172,157 , GRCh37.p13 chr21: 47,592,004-47,592,071 SPATC1L
    nsv7029910copy number variation1nstd229human GRCh38 chr21: 46,015,310-46,317,714 , GRCh37.p13 chr21: 47,435,224-47,737,628 MCM3AP, C21orf58, 10 more genes
    nsv7028269copy number variation1nstd229human GRCh38 chr21: 46,173,489-46,186,096 , GRCh37.p13 chr21: 47,593,403-47,606,010 SPATC1L
    nsv7027524copy number variation1nstd229human GRCh38 chr21: 46,158,292-46,165,397 , GRCh37.p13 chr21: 47,578,206-47,585,311 SPATC1L
    nsv7024185copy number variation1nstd229human GRCh38 chr21: 46,161,032-46,162,995 , GRCh37.p13 chr21: 47,580,946-47,582,909 SPATC1L
    nsv7021733copy number variation1nstd229human GRCh38 chr21: 46,008,378-46,181,422 , GRCh37.p13 chr21: 47,428,292-47,601,336 FTCD-AS1, FTCD, 4 more genes
    nsv7020831copy number variation1nstd229human GRCh38 chr21: 46,179,735-46,186,213 , GRCh37.p13 chr21: 47,599,649-47,606,127 SPATC1L
    nsv7020683copy number variation1nstd229human GRCh38 chr21: 46,090,901-46,241,100 , GRCh37.p13 chr21: 47,510,815-47,661,014 FTCD-AS1, MCM3AP-AS1, 6 more genes
    nsv7020575copy number variation1nstd229human GRCh38 chr21: 46,012,321-46,209,150 , GRCh37.p13 chr21: 47,432,235-47,629,064 SPATC1L, PSMA6P3, 6 more genes
    nsv7018527copy number variation1nstd229human GRCh38 chr21: 46,135,901-46,161,500 , GRCh37.p13 chr21: 47,555,815-47,581,414 FTCD, FTCD-AS1, 1 more genes
    nsv6637891copy number variation1nstd102humanUncertain significance GRCh37 chr21: 46,882,064-47,963,149 , GRCh38.p12 chr21: 45,462,150-46,543,236 C21orf58, PCNT, 25 more genes
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