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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094684copy number variation1nstd102humanPathogenic GRCh37 chr16: 68,349,883-68,732,303 , GRCh38.p12 chr16: 68,315,980-68,698,400 LOC105371321, RNU4-30P, 8 more genes
    nsv7094683copy number variation1nstd102humanUncertain significance GRCh37 chr16: 65,821,800-72,146,396 , GRCh38.p12 chr16: 65,787,897-72,112,497 TRG-GCC5-1, RNU6-359P, 205 more genes
    nsv7075094inversion1nstd229human GRCh38 chr16: 67,913,190-69,541,641 , GRCh37.p13 chr16: 67,947,093-69,575,544 PSMB10, COG8, 52 more genes
    nsv7075084inversion1nstd229human GRCh38 chr16: 67,127,296-73,957,488 , GRCh37.p13 chr16: 67,161,199-73,991,387 MIR1538, LINC02136, 187 more genes
    nsv7058675inversion1nstd229human GRCh38 chr16: 67,667,666-75,720,241 , GRCh37.p13 chr16: 67,701,569-75,754,139 RNU6-898P, DPEP2, 199 more genes
    nsv6994280copy number variation1nstd229human GRCh38 chr16: 68,551,312-68,555,166 , GRCh37.p13 chr16: 68,585,215-68,589,069 ZFP90
    nsv6986762copy number variation1nstd229human GRCh38 chr16: 68,549,254-68,714,434 , GRCh37.p13 chr16: 68,583,157-68,748,337 CDH3, HSPE1P5, 2 more genes
    nsv6986213copy number variation1nstd229human GRCh38 chr16: 68,527,367-68,530,823 , GRCh37.p13 chr16: 68,561,270-68,564,726 ZFP90
    nsv6984867copy number variation1nstd229human GRCh38 chr16: 68,533,445-68,563,633 , GRCh37.p13 chr16: 68,567,348-68,597,536 ZFP90, RNU4-36P
    nsv6984562copy number variation1nstd229human GRCh38 chr16: 68,391,642-68,592,950 , GRCh37.p13 chr16: 68,425,545-68,626,853 RPL35AP33, LOC105371321, 3 more genes
    nsv6984339copy number variation1nstd229human GRCh38 chr16: 68,379,164-68,807,023 , GRCh37.p13 chr16: 68,413,067-68,840,926 CDH1, SMPD3, 8 more genes
    nsv6982666copy number variation1nstd229human GRCh38 chr16: 68,541,758-68,546,388 , GRCh37.p13 chr16: 68,575,661-68,580,291 ZFP90
    nsv6980619copy number variation1nstd229human GRCh38 chr16: 68,566,607-68,566,757 , GRCh37.p13 chr16: 68,600,510-68,600,660 ZFP90
    nsv6979734copy number variation1nstd229human GRCh38 chr16: 68,564,512-68,568,178 , GRCh37.p13 chr16: 68,598,415-68,602,081 ZFP90
    nsv6637199copy number variation1nstd102humanUncertain significance GRCh37 chr16: 68,326,200-68,970,975 , GRCh38.p12 chr16: 68,292,297-68,937,072 HSPE1P5, RPL35AP33, 15 more genes
    nsv6576736inversion1nstd223human GRCh38 chr16: 68,545,870-68,546,694 , GRCh37.p13 chr16: 68,579,773-68,580,597 ZFP90
    nsv6514923copy number variation1nstd223human GRCh38 chr16: 68,531,956-68,534,641 , GRCh37.p13 chr16: 68,565,859-68,568,544 ZFP90, RNU4-36P
    nsv6514390copy number variation1nstd223human GRCh38 chr16: 68,545,101-68,548,800 , GRCh37.p13 chr16: 68,579,004-68,582,703 ZFP90
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
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