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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5644492insertion1nstd207human GRCh38 chr8: 144,505,532-144,505,532 , GRCh37.p13 chr8: 145,730,915-145,730,915 LOC101928953, GPT
    nsv5248548copy number variation1nstd204human GRCh38.p13 chr8: 143,866,301-144,531,400 , GRCh37.p13 chr8: 145,146,063-145,756,784 MIR661, EXOSC4, 51 more genes
    nsv4829377copy number variation1nstd200human GRCh37 chr8: 145,677,518-145,742,837 , GRCh38.p12 chr8: 144,452,135-144,517,453 MIR10400, LRRC14, 8 more genes
    nsv4769373copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,033,244-146,297,937 , GRCh38.p12 chr8: 143,959,076-145,072,551 ZFTRAF1, PLEC, 68 more genes
    nsv4729603copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 144,262,042-146,295,771 , GRCh38.p12 chr8: 143,180,625-145,070,385 CYC1, EEF1D, 112 more genes
    nsv4729346copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,555,125-145,779,806 , GRCh38.p12 chr8: 144,331,462-144,554,422 FOXH1, MIR10400, 26 more genes
    nsv4675664copy number variation1nstd102humanPathogenic GRCh37 chr8: 128,877,995-146,295,771 , GRCh38.p12 chr8: 127,865,749-145,070,385 LOC105375789, LINC02990, 270 more genes
    nsv4675273copy number variation1nstd102humanPathogenic GRCh37 chr8: 121,042,467-146,295,771 , GRCh38.p12 chr8: 120,030,228-145,070,385 TOP1MT, SLA, 379 more genes
    nsv4668214copy number variation1nstd186human GRCh37 chr8: 145,726,184-145,726,587 , GRCh38.p12 chr8: 144,500,801-144,501,204 GPT, PPP1R16A, 1 more genes
    nsv4617224copy number variation1nstd183human GRCh37 chr8: 145,725,665-145,725,785 , GRCh38.p12 chr8: 144,500,282-144,500,402 GPT, PPP1R16A, 1 more genes
    nsv4614846copy number variation1nstd183human GRCh37 chr8: 145,726,184-145,726,587 , GRCh38.p12 chr8: 144,500,801-144,501,204 PPP1R16A, LOC101928953, 1 more genes
    nsv4611337copy number variation1nstd183human GRCh37 chr8: 145,726,184-145,726,243 , GRCh38.p12 chr8: 144,500,801-144,500,860 GPT, PPP1R16A, 1 more genes
    nsv4608945copy number variation1nstd183human GRCh37 chr8: 145,725,665-145,725,724 , GRCh38.p12 chr8: 144,500,282-144,500,341 GPT, PPP1R16A, 1 more genes
    nsv4605585copy number variation1nstd183human GRCh37 chr8: 145,725,665-145,726,541 , GRCh38.p12 chr8: 144,500,282-144,501,158 GPT, PPP1R16A, 1 more genes
    nsv4602995copy number variation1nstd183human GRCh37 chr8: 145,722,093-145,726,080 , GRCh38.p12 chr8: 144,496,710-144,500,697 GPT, PPP1R16A, 1 more genes
    nsv4599460copy number variation1nstd183human GRCh37 chr8: 145,567,872-145,904,090 , GRCh38.p12 chr8: 144,344,210-144,678,705 RECQL4, ZFTRAF1, 25 more genes
    nsv4457078copy number variation1nstd102humanPathogenic GRCh37 chr8: 139,188,797-146,295,771 , GRCh38.p12 chr8: 138,176,554-145,070,385 GSDMD, MROH1, 181 more genes
    nsv4456997copy number variation1nstd102humanPathogenic GRCh37 chr8: 125,496,223-146,295,771 , GRCh38.p12 chr8: 124,483,982-145,070,385 LOC107986906, GPIHBP1, 317 more genes
    nsv4456942copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,695,493-145,798,535 , GRCh38.p12 chr8: 144,470,110-144,573,151 LOC101928953, KIFC2, 9 more genes
    nsv4456937copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,645,435-145,881,333 , GRCh38.p12 chr8: 144,431,464-144,655,948 LRRC14, RECQL4, 14 more genes
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