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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077330inversion1nstd229human GRCh38 chr21: 20,333,755-29,497,356 , GRCh37.p13 chr21: 21,706,067-30,869,676 LOC105372770, LOC100419737, 95 more genes
    nsv7071358inversion1nstd229human GRCh38 chr21: 23,691,748-31,155,798 , GRCh37.p13 chr21: 25,064,065-32,528,116 LLPHP2, KRTAP20-3, 126 more genes
    nsv7070554inversion1nstd229human GRCh38 chr21: 28,138,154-35,660,050 , GRCh37.p13 chr21: 29,510,473-37,032,348 , OR7E23P, 160 more genes
    nsv7070253inversion1nstd229human GRCh38 chr21: 28,377,443-35,730,342 , GRCh37.p13 chr21: 29,749,764-37,102,640 , HUNK, 161 more genes
    nsv7065590inversion1nstd229human GRCh38 chr21: 23,756,613-30,931,318 , GRCh37.p13 chr21: 25,128,930-32,303,637 LINC01697, LOC105372753, 119 more genes
    nsv7059344inversion1nstd229human GRCh38 chr21: 28,609,769-29,034,163 , GRCh37.p13 chr21: 29,982,091-30,406,484 LTN1, HSPD1P7, 6 more genes
    nsv7033618copy number variation1nstd229human GRCh38 chr21: 28,549,601-29,037,287 , GRCh37.p13 chr21: 29,921,923-30,409,608 LTN1, USP16, 6 more genes
    nsv7027896copy number variation1nstd229human GRCh38 chr21: 29,016,190-29,035,240 , GRCh37.p13 chr21: 30,388,511-30,407,561 USP16, RWDD2B
    nsv7026522copy number variation1nstd229human GRCh38 chr21: 29,045,301-29,050,400 , GRCh37.p13 chr21: 30,417,622-30,422,721 USP16
    nsv7023945copy number variation1nstd229human GRCh38 chr21: 27,856,301-31,095,924 , GRCh37.p13 chr21: 29,228,620-32,468,242 KRTAP19-11P, KRTAP6-2, 78 more genes
    nsv7022452copy number variation1nstd229human GRCh38 chr21: 28,954,810-29,071,458 , GRCh37.p13 chr21: 30,327,132-30,443,779 LOC105372766, LTN1, 4 more genes
    nsv7020182copy number variation1nstd229human GRCh38 chr21: 28,984,601-29,030,100 , GRCh37.p13 chr21: 30,356,922-30,402,421 USP16, LTN1, 3 more genes
    nsv7018731copy number variation1nstd229human GRCh38 chr21: 29,052,744-29,052,914 , GRCh37.p13 chr21: 30,425,065-30,425,235 USP16
    nsv6637343copy number variation1nstd102humanUncertain significance GRCh37 chr21: 29,243,314-32,472,073 , GRCh38.p12 chr21: 27,870,995-31,099,755 GAPDHP14, LINC00189, 78 more genes
    nsv6626624copy number variation1nstd224human GRCh37 chr21: 1-48,129,895 , GRCh38.p12 chr21: 8,522,361-46,699,983 , ATP5PO, 657 more genes
    nsv6599271inversion1nstd223human GRCh38 chr21: 29,047,777-29,047,927 , GRCh37.p13 chr21: 30,420,098-30,420,248 USP16
    nsv6596327inversion1nstd223human GRCh38 chr21: 28,377,391-35,730,332 , GRCh37.p13 chr21: 29,749,712-37,102,630 , LOC107985515, 161 more genes
    nsv6595911inversion1nstd223human GRCh38 chr21: 29,028,601-29,029,225 , GRCh37.p13 chr21: 30,400,922-30,401,546 USP16
    nsv6539369copy number variation1nstd223human GRCh38 chr21: 29,026,250-29,029,142 , GRCh37.p13 chr21: 30,398,571-30,401,463 USP16
    nsv6315551copy number variation1nstd102humanPathogenic GRCh37 chr21: 14,420,615-48,080,926 , GRCh38.p12 chr21: 13,048,294-46,661,014 LTN1, LOC105372740, 622 more genes
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