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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5920360copy number variation1nstd209human GRCh38 chr8: 144,492,586-144,495,686 , GRCh37.p13 chr8: 145,717,969-145,721,069 LOC101928953, PPP1R16A
    nsv5851050copy number variation1nstd209human GRCh38 chr8: 144,492,553-144,495,652 , GRCh37.p13 chr8: 145,717,936-145,721,035 PPP1R16A, LOC101928953
    nsv5695767mobile element insertion1nstd211human GRCh38 chr8: 144,499,178-144,499,178 , GRCh37.p13 chr8: 145,724,561-145,724,561 PPP1R16A, LOC101928953
    nsv5483435copy number variation1nstd206human GRCh38 chr8: 144,494,577-144,495,683 , GRCh37.p13 chr8: 145,719,960-145,721,066 LOC101928953, PPP1R16A
    nsv5480068copy number variation1nstd206human GRCh38 chr8: 144,492,623-144,495,687 , GRCh37.p13 chr8: 145,718,006-145,721,070 PPP1R16A, LOC101928953
    nsv5478483copy number variation1nstd206human GRCh38 chr8: 144,492,490-144,494,425 , GRCh37.p13 chr8: 145,717,873-145,719,808 LOC101928953, PPP1R16A
    nsv5253246copy number variation1nstd204human GRCh38.p13 chr8: 144,492,278-144,495,577 , GRCh37.p13 chr8: 145,717,661-145,720,960 PPP1R16A, LOC101928953
    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
    nsv5246641copy number variation1nstd204human GRCh38.p13 chr8: 144,492,501-144,495,700 , GRCh37.p13 chr8: 145,717,884-145,721,083 PPP1R16A, LOC101928953
    nsv5241795copy number variation1nstd204human GRCh38.p13 chr8: 144,468,549-144,478,418 , GRCh37.p13 chr8: 145,693,932-145,703,801 FOXH1, PPP1R16A, 1 more genes
    nsv4969175copy number variation1nstd200human GRCh38 chr8: 144,480,570-144,495,607 , GRCh37.p13 chr8: 145,705,953-145,720,990 LOC101928953, PPP1R16A
    nsv4962719copy number variation1nstd200human GRCh38 chr8: 144,492,626-144,495,621 , GRCh37.p13 chr8: 145,718,009-145,721,004 PPP1R16A, LOC101928953
    nsv4962718copy number variation1nstd200human GRCh38 chr8: 144,486,610-144,486,718 , GRCh37.p13 chr8: 145,711,993-145,712,101 PPP1R16A
    nsv4962717copy number variation1nstd200human GRCh38 chr8: 144,481,172-144,492,537 , GRCh37.p13 chr8: 145,706,555-145,717,920 LOC101928953, PPP1R16A
    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
    nsv4813921copy number variation1nstd200human GRCh37 chr8: 145,702,688-145,705,911 , GRCh38.p12 chr8: 144,477,305-144,480,528 PPP1R16A
    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
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