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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137191copy number variation1nstd102humanPathogenic GRCh37 chr1: 1,957,148-6,553,454 , GRCh38.p12 chr1: 2,025,709-6,493,394 LOC102724429, TNFRSF14, 86 more genes
    nsv7137068copy number variation1nstd102humanLikely benign GRCh37 chr1: 2,567,832-3,209,952 , GRCh38.p12 chr1: 2,636,393-3,293,388 PRDM16, LOC107984904, 16 more genes
    nsv7137045copy number variation1nstd102humanPathogenic GRCh37 chr1: 536,777-6,012,896 , GRCh38.p12 chr1: 601,397-5,952,836 MIR200B, LOC105378608, 172 more genes
    nsv7098948copy number variation1nstd102humanUncertain significance GRCh38 chr1: 2,518,272-4,413,203 , GRCh37.p13 chr1: 2,449,711-4,473,263 LOC107984904, DFFB, 46 more genes
    nsv7058041inversion1nstd229human GRCh38 chr1: 1,845,355-9,534,096 , GRCh37.p13 chr1: 1,776,794-9,594,155 RPL37P9, TMEM52, 152 more genes
    nsv7054534inversion1nstd229human GRCh38 chr1: 2,972,403-10,562,308 , GRCh37.p13 chr1: 2,888,967-10,622,365 RN7SL731P, LOC105376682, 145 more genes
    nsv7053857inversion1nstd229human GRCh38 chr1: 3,058,591-3,061,850 , GRCh37.p13 chr1: 2,975,155-2,978,414 PRDM16-DT
    nsv7051203inversion1nstd229human GRCh38 chr1: 2,476,867-3,696,891 , GRCh37.p13 chr1: 2,408,306-3,613,455 TP73, PRXL2B, 33 more genes
    nsv7045845inversion1nstd229human GRCh38 chr1: 3,052,091-3,069,061 , GRCh37.p13 chr1: 2,968,655-2,985,625 PRDM16, LOC100420339, 1 more genes
    nsv6648603copy number variation1nstd229human GRCh38 chr1: 3,056,470-3,061,086 , GRCh37.p13 chr1: 2,973,034-2,977,650 PRDM16-DT
    nsv6648601copy number variation1nstd229human GRCh38 chr1: 3,052,090-3,064,520 , GRCh37.p13 chr1: 2,968,654-2,981,084 PRDM16-DT
    nsv6648465copy number variation1nstd229human GRCh38 chr1: 3,067,801-3,071,100 , GRCh37.p13 chr1: 2,984,365-2,987,664 PRDM16-DT, PRDM16, 1 more genes
    nsv6648461copy number variation1nstd229human GRCh38 chr1: 3,059,081-3,067,491 , GRCh37.p13 chr1: 2,975,645-2,984,055 PRDM16-DT, PRDM16
    nsv6648440copy number variation1nstd229human GRCh38 chr1: 3,004,990-3,396,785 , GRCh37.p13 chr1: 2,921,554-3,313,349 LOC105378604, PRDM16, 7 more genes
    nsv6648386copy number variation1nstd229human GRCh38 chr1: 2,999,698-3,124,285 , GRCh37.p13 chr1: 2,916,262-3,040,849 PRDM16, LOC100420339, 2 more genes
    nsv6647946copy number variation1nstd229human GRCh38 chr1: 2,998,246-3,073,575 , GRCh37.p13 chr1: 2,914,810-2,990,139 PRDM16-DT, LOC100420339, 2 more genes
    nsv6647879copy number variation1nstd229human GRCh38 chr1: 2,800,201-3,815,100 , GRCh37.p13 chr1: 2,716,766-3,731,664 CEP104, PRDM16-DT, 22 more genes
    nsv6637093copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897 VWA1, CEP104, 311 more genes
    nsv6637067copy number variation1nstd102humanUncertain significance GRCh37 chr1: 2,974,212-4,408,415 , GRCh38.p12 chr1: 3,057,648-4,348,355 LRRC47, LOC105378605, 27 more genes
    nsv6636594copy number variation1nstd102humanUncertain significance GRCh37 chr1: 2,628,158-3,191,234 , GRCh38.p12 chr1: 2,696,719-3,274,670 PRDM16, LOC105378599, 15 more genes
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