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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140931insertion1nstd232human GRCh37.p13 chr1: 3,737,058-3,737,058 , GRCh38.p12 chr1: 3,820,494-3,820,494 CEP104
    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
    nsv7137045copy number variation1nstd102humanPathogenic GRCh37 chr1: 536,777-6,012,896 , GRCh38.p12 chr1: 601,397-5,952,836 MIR200B, LOC105378608, 172 more genes
    nsv7099174copy number variation1nstd231human GRCh38.p12 chr1: 3,752,749-6,208,083 , GRCh37 chr1: 3,669,313-6,268,143 DFFB, RPL22, 27 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
    nsv7042068inversion1nstd229human GRCh38 chr1: 3,820,027-3,820,078 , GRCh37.p13 chr1: 3,736,591-3,736,642 CEP104
    nsv6649620copy number variation1nstd229human GRCh38 chr1: 3,824,739-3,829,100 , GRCh37.p13 chr1: 3,741,303-3,745,664 CEP104
    nsv6649215copy number variation1nstd229human GRCh38 chr1: 3,532,130-4,419,144 , GRCh37.p13 chr1: 3,448,694-4,479,204 LINC02780, MIR551A, 19 more genes
    nsv6649096copy number variation1nstd229human GRCh38 chr1: 3,840,818-3,844,040 , GRCh37.p13 chr1: 3,757,382-3,760,604 CEP104
    nsv6649084copy number variation1nstd229human GRCh38 chr1: 3,801,351-3,810,942 , GRCh37.p13 chr1: 3,717,915-3,727,506 CEP104
    nsv6649077copy number variation1nstd229human GRCh38 chr1: 3,787,637-3,856,537 , GRCh37.p13 chr1: 3,704,201-3,773,101 LRRC47, CEP104, 1 more genes
    nsv6648783copy number variation1nstd229human GRCh38 chr1: 3,557,253-4,081,288 , GRCh37.p13 chr1: 3,473,817-4,141,348 LINC02780, MEGF6, 16 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
    nsv6636408copy number variation1nstd102humanUncertain significance GRCh37 chr1: 2,194,087-4,738,355 , GRCh38.p12 chr1: 2,262,648-4,678,295 LINC01777, LOC105378606, 55 more genes
    nsv6636399copy number variation1nstd102humanPathogenic GRCh37 chr1: 2,173,570-5,023,430 , GRCh38.p12 chr1: 2,242,131-4,963,370 LOC105378602, MORN1, 55 more genes
    nsv6546059inversion1nstd223human GRCh38 chr1: 3,843,512-3,844,582 , GRCh37.p13 chr1: 3,760,076-3,761,146 CEP104
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