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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148175copy number variation1nstd102humanPathogenic GRCh38 chr1: 230,178,121-243,646,135 , GRCh37.p13 chr1: 230,313,867-243,809,437 AGT, MAP10, 221 more genes
    nsv7148158copy number variation1nstd102humanPathogenic GRCh38 chr1: 235,215,476-247,005,888 , GRCh37.p13 chr1: 235,378,791-247,169,190 RNU6-747P, LINC01139, 172 more genes
    nsv7147142insertion1nstd232human GRCh37.p13 chr1: 236,145,084-236,145,084 , GRCh38.p12 chr1: 235,981,784-235,981,784 NID1
    nsv7141320insertion1nstd232human GRCh37.p13 chr1: 236,201,553-236,201,553 , GRCh38.p12 chr1: 236,038,253-236,038,253 NID1
    nsv7137173copy number variation1nstd102humanPathogenic GRCh38 chr1: 233,502,994-236,105,019 , GRCh37.p13 chr1: 233,638,740-236,268,319 ARID4B, MTND3P8, 58 more genes
    nsv7093371copy number variation1nstd102humannot provided GRCh37 chr1: 224,230,307-243,181,599 , GRCh38.p12 chr1: 224,042,605-243,018,297 RPL36P6, MTND4LP21, 377 more genes
    nsv7044547inversion1nstd229human GRCh38 chr1: 234,053,817-240,091,334 , GRCh37.p13 chr1: 234,189,563-240,254,634 RNU6-725P, RNU6-968P, 101 more genes
    nsv7040505inversion1nstd229human GRCh38 chr1: 235,226,873-236,268,697 , GRCh37.p13 chr1: 235,390,188-236,431,997 RPS21P1, NID1, 26 more genes
    nsv6673890copy number variation1nstd229human GRCh38 chr1: 236,003,489-236,003,941 , GRCh37.p13 chr1: 236,166,789-236,167,241 NID1
    nsv6672380copy number variation1nstd229human GRCh38 chr1: 235,981,801-235,986,000 , GRCh37.p13 chr1: 236,145,101-236,149,300 NID1
    nsv6669540copy number variation1nstd229human GRCh38 chr1: 235,997,093-236,000,659 , GRCh37.p13 chr1: 236,160,393-236,163,959 NID1
    nsv6664488copy number variation1nstd229human GRCh38 chr1: 236,055,105-236,059,021 , GRCh37.p13 chr1: 236,218,405-236,222,321 NID1
    nsv6664309copy number variation1nstd229human GRCh38 chr1: 235,978,017-235,978,920 , GRCh37.p13 chr1: 236,141,317-236,142,220 NID1
    nsv6660689copy number variation1nstd229human GRCh38 chr1: 235,809,012-236,113,984 , GRCh37.p13 chr1: 235,972,312-236,277,284 LINC02768, LOC105373215, 6 more genes
    nsv6659973copy number variation1nstd229human GRCh38 chr1: 235,759,310-236,025,592 , GRCh37.p13 chr1: 235,922,610-236,188,892 RNU5E-2P, RNU6-968P, 5 more genes
    nsv6659688copy number variation1nstd229human GRCh38 chr1: 235,760,337-236,349,480 , GRCh37.p13 chr1: 235,923,637-236,512,780 LOC100130485, RNU6-968P, 10 more genes
    nsv6637109copy number variation1nstd102humanUncertain significance GRCh37 chr1: 232,895,447-238,787,061 , GRCh38.p12 chr1: 232,759,701-238,623,761 RPL9P10, LOC105373207, 105 more genes
    nsv6637037copy number variation1nstd102humanUncertain significance GRCh37 chr1: 232,827,966-240,750,334 , GRCh38.p12 chr1: 232,692,220-240,587,034 RNU1-74P, EDARADD, 123 more genes
    nsv6636794copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,972,939-249,224,684 , GRCh38.p12 chr1: 223,785,237-248,930,485 SEPTIN7P13, WNT3A, 546 more genes
    nsv6636586copy number variation1nstd102humanUncertain significance GRCh37 chr1: 236,023,942-236,388,093 , GRCh38.p12 chr1: 235,860,642-236,224,793 LOC343508, LOC105373215, 7 more genes
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