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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099181copy number variation1nstd231human GRCh38.p12 chr1: 18,899,486-20,046,918 , GRCh37 chr1: 19,225,980-20,373,411 CAPZB, HTR6, 32 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7095949copy number variation1nstd102humanUncertain significance GRCh37 chr1: 19,199,339-24,690,861 , GRCh38.p12 chr1: 18,872,845-24,364,371 RPL29P6, NBPF3, 156 more genes
    nsv7095496copy number variation3nstd102humanUncertain significance GRCh37 chr1: 19,199,339-22,987,879 , GRCh38.p12 chr1: 18,872,845-22,661,386 RN7SL277P, MPHOSPH6P1, 103 more genes
    nsv7049927inversion1nstd229human GRCh38 chr1: 12,447,483-21,286,051 , GRCh37.p13 chr1: 12,507,539-21,612,544 SLC25A34, RNA5SP41, 238 more genes
    nsv7044339inversion1nstd229human GRCh38 chr1: 20,036,510-20,036,533 , GRCh37.p13 chr1: 20,363,003-20,363,026 PLA2G5
    nsv7044199inversion1nstd229human GRCh38 chr1: 20,051,725-20,078,918 , GRCh37.p13 chr1: 20,378,218-20,405,411 PLA2G5
    nsv6647140copy number variation1nstd229human GRCh38 chr1: 20,089,201-20,103,600 , GRCh37.p13 chr1: 20,415,694-20,430,093 PLA2G5
    nsv6646972copy number variation1nstd229human GRCh38 chr1: 20,080,593-20,084,195 , GRCh37.p13 chr1: 20,407,086-20,410,688 PLA2G5
    nsv6646971copy number variation1nstd229human GRCh38 chr1: 20,068,357-20,068,409 , GRCh37.p13 chr1: 20,394,850-20,394,902 PLA2G5
    nsv6646968copy number variation1nstd229human GRCh38 chr1: 20,041,655-20,050,279 , GRCh37.p13 chr1: 20,368,148-20,376,772 PLA2G5
    nsv6646899copy number variation1nstd229human GRCh38 chr1: 19,751,232-20,412,088 , GRCh37.p13 chr1: 20,077,725-20,738,581 LOC105376826, LOC105376823, 17 more genes
    nsv6646828copy number variation1nstd229human GRCh38 chr1: 20,090,301-20,093,800 , GRCh37.p13 chr1: 20,416,794-20,420,293 PLA2G5
    nsv6646827copy number variation1nstd229human GRCh38 chr1: 20,080,592-20,088,158 , GRCh37.p13 chr1: 20,407,085-20,414,651 PLA2G5
    nsv6646826copy number variation1nstd229human GRCh38 chr1: 20,077,473-20,077,596 , GRCh37.p13 chr1: 20,403,966-20,404,089 PLA2G5
    nsv6646825copy number variation1nstd229human GRCh38 chr1: 20,072,355-20,092,625 , GRCh37.p13 chr1: 20,398,848-20,419,118 PLA2G5
    nsv6646453copy number variation1nstd229human GRCh38 chr1: 20,021,142-20,030,204 , GRCh37.p13 chr1: 20,347,635-20,356,697 PLA2G5
    nsv6544252inversion1nstd223human GRCh38 chr1: 20,059,140-20,060,298 , GRCh37.p13 chr1: 20,385,633-20,386,791 PLA2G5
    nsv6539450inversion1nstd223human GRCh38 chr1: 20,060,461-20,061,562 , GRCh37.p13 chr1: 20,386,954-20,388,055 PLA2G5
    nsv6335507copy number variation1nstd223human GRCh38 chr1: 20,072,204-20,074,365 , GRCh37.p13 chr1: 20,398,697-20,400,858 PLA2G5
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