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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077602inversion1nstd229human GRCh38 chr12: 132,975,813-132,994,248 , GRCh37.p13 chr12: 133,552,399-133,570,834 RNU4ATAC12P, ZNF26
    nsv7076223inversion1nstd229human GRCh38 chr12: 132,900,540-133,122,270 , GRCh37.p13 chr12: 133,477,126-133,698,856 ZNF605, ZNF140, 8 more genes
    nsv7071120inversion1nstd229human GRCh38 chr12: 132,918,120-132,985,001 , GRCh37.p13 chr12: 133,494,706-133,561,587 ZNF605, ZNF26, 1 more genes
    nsv6937093copy number variation1nstd229human GRCh38 chr12: 132,991,898-132,992,233 , GRCh37.p13 chr12: 133,568,484-133,568,819 ZNF26
    nsv6936139copy number variation1nstd229human GRCh38 chr12: 132,988,144-133,005,876 , GRCh37.p13 chr12: 133,564,730-133,582,462 RNU4ATAC12P, ZNF26
    nsv6934654copy number variation1nstd229human GRCh38 chr12: 132,501,807-133,106,378 , GRCh37.p13 chr12: 133,078,393-133,682,964 ZNF605, LRCOL1, 23 more genes
    nsv6933781copy number variation1nstd229human GRCh38 chr12: 133,007,438-133,011,684 , GRCh37.p13 chr12: 133,584,024-133,588,270 ZNF26
    nsv6933437copy number variation1nstd229human GRCh38 chr12: 132,992,285-132,997,668 , GRCh37.p13 chr12: 133,568,871-133,574,254 ZNF26, RNU4ATAC12P
    nsv6933003copy number variation1nstd229human GRCh38 chr12: 133,006,701-133,018,300 , GRCh37.p13 chr12: 133,583,287-133,594,886 ZNF26
    nsv6930953copy number variation1nstd229human GRCh38 chr12: 132,924,448-133,112,061 , GRCh37.p13 chr12: 133,501,034-133,688,647 ZNF140, PTP4A1P2, 6 more genes
    nsv6930944copy number variation1nstd229human GRCh38 chr12: 132,932,701-132,993,800 , GRCh37.p13 chr12: 133,509,287-133,570,386 ZNF26, RNU4ATAC12P, 2 more genes
    nsv6928129copy number variation1nstd229human GRCh38 chr12: 133,016,572-133,030,673 , GRCh37.p13 chr12: 133,593,158-133,607,259 ZNF84-DT, ZNF26
    nsv6927192copy number variation1nstd229human GRCh38 chr12: 132,980,725-133,006,690 , GRCh37.p13 chr12: 133,557,311-133,583,276 ZNF26, RNU4ATAC12P
    nsv6925912copy number variation1nstd229human GRCh38 chr12: 132,971,691-132,985,571 , GRCh37.p13 chr12: 133,548,277-133,562,157 ZNF26, NANOGNBP2
    nsv6923679copy number variation1nstd229human GRCh38 chr12: 132,987,386-132,993,183 , GRCh37.p13 chr12: 133,563,972-133,569,769 ZNF26
    nsv6923569copy number variation1nstd229human GRCh38 chr12: 132,987,545-132,990,078 , GRCh37.p13 chr12: 133,564,131-133,566,664 ZNF26
    nsv6921620copy number variation1nstd229human GRCh38 chr12: 132,990,096-132,995,865 , GRCh37.p13 chr12: 133,566,682-133,572,451 RNU4ATAC12P, ZNF26
    nsv6920131copy number variation1nstd229human GRCh38 chr12: 132,719,848-132,999,769 , GRCh37.p13 chr12: 133,296,434-133,576,355 RNU4ATAC12P, ZNF26, 12 more genes
    nsv6918272copy number variation1nstd229human GRCh38 chr12: 133,017,732-133,017,866 , GRCh37.p13 chr12: 133,594,318-133,594,452 ZNF26
    nsv6918267copy number variation1nstd229human GRCh38 chr12: 132,997,893-133,004,179 , GRCh37.p13 chr12: 133,574,479-133,580,765 ZNF26
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