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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
    nsv7099175copy number variation1nstd231human GRCh38.p12 chr1: 6,492,665-9,894,222 , GRCh37 chr1: 6,552,725-9,954,280 RERE, CA6, 70 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
    nsv7095630copy number variation1nstd102humanUncertain significance GRCh37 chr1: 6,527,623-6,537,631 , GRCh38.p12 chr1: 6,467,563-6,477,571 PLEKHG5
    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
    nsv7052066inversion1nstd229human GRCh38 chr1: 4,379,650-7,782,927 , GRCh37.p13 chr1: 4,439,710-7,842,987 NPHP4, MIR4252, 46 more genes
    nsv7047983inversion1nstd229human GRCh38 chr1: 5,346,988-12,521,611 , GRCh37.p13 chr1: 5,407,048-12,581,655 THAP3, UBIAD1, 165 more genes
    nsv7046461inversion1nstd229human GRCh38 chr1: 5,352,168-12,521,473 , GRCh37.p13 chr1: 5,412,228-12,581,517 LINC02606, C1orf127, 165 more genes
    nsv6653411copy number variation1nstd229human GRCh38 chr1: 6,487,982-6,488,271 , GRCh37.p13 chr1: 6,548,042-6,548,331 PLEKHG5
    nsv6653193copy number variation1nstd229human GRCh38 chr1: 6,517,099-6,517,133 , GRCh37.p13 chr1: 6,577,159-6,577,193 PLEKHG5
    nsv6653101copy number variation1nstd229human GRCh38 chr1: 6,506,101-6,515,900 , GRCh37.p13 chr1: 6,566,161-6,575,960 PLEKHG5
    nsv6652673copy number variation1nstd229human GRCh38 chr1: 6,520,417-6,587,903 , GRCh37.p13 chr1: 6,580,477-6,647,963 LOC107984912, TAS1R1, 4 more genes
    nsv6652430copy number variation1nstd229human GRCh38 chr1: 6,459,901-6,477,600 , GRCh37.p13 chr1: 6,519,961-6,537,660 TNFRSF25, PLEKHG5, 1 more genes
    nsv6652385copy number variation1nstd229human GRCh38 chr1: 6,319,996-6,482,757 , GRCh37.p13 chr1: 6,380,056-6,542,817 TNFRSF25, MIR4252, 4 more genes
    nsv6652370copy number variation1nstd229human GRCh38 chr1: 6,261,636-6,608,517 , GRCh37.p13 chr1: 6,321,696-6,668,577 LOC107984913, ZBTB48, 11 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
    nsv6636950copy number variation1nstd102humanPathogenic GRCh37 chr1: 5,505,039-7,027,995 , GRCh38.p12 chr1: 5,444,979-6,967,935 RPL37P9, PHF13, 31 more genes
    nsv6333326copy number variation1nstd223human GRCh38 chr1: 6,494,186-6,496,034 , GRCh37.p13 chr1: 6,554,246-6,556,094 PLEKHG5
    nsv6329098copy number variation1nstd223human GRCh38 chr1: 6,520,417-6,587,903 , GRCh37.p13 chr1: 6,580,477-6,647,963 PLEKHG5, NOL9, 4 more genes
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