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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5631803insertion1nstd207human GRCh38 chr8: 143,569,279-143,569,279 , GRCh37.p13 chr8: 144,651,449-144,651,449 MROH6
    nsv5337768translocation1nstd200human GRCh37 chr3: 48,533,403-48,533,403 , GRCh37 chr8: 144,646,735-144,646,735 , GRCh38.p9 chr: NaN-NaN , GRCh38.p12 chr: NaN-NaN , GRCh38.p12 chr8|NT_187571.1: 54,605-54,605 , GRCh38.p12 chr8: 143,564,565-143,564,565 MROH6
    nsv5315113copy number variation1nstd204human GRCh37.p13 chr8: 144,652,746-144,655,730 , GRCh38.p13 chr8: 143,570,576-143,573,560 NAPRT, MROH6
    nsv5301183copy number variation1nstd204human GRCh38.p13 chr8: 143,160,494-143,803,360 , GRCh37.p13 chr8: 144,241,911-144,743,529 TIGD5, MAPK15, 36 more genes
    nsv5258736copy number variation1nstd204human GRCh38.p13 chr8: 143,570,063-143,573,427 , GRCh37.p13 chr8: 144,652,233-144,655,597 NAPRT, MROH6
    nsv5254948copy number variation1nstd204human GRCh38.p13 chr8: 143,167,001-143,860,200 , GRCh37.p13 chr8: 144,248,418-144,743,525 LOC105375798, LINC02990, 41 more genes
    nsv5250708copy number variation1nstd204human GRCh37.p13 chr8: 144,636,271-144,700,470 , GRCh38.p13 chr8: 143,554,101-143,618,300 EEF1D, GFUS, 6 more genes
    nsv4962646copy number variation1nstd200human GRCh38 chr8: 143,566,393-143,567,584 , GRCh37.p13 chr8: 144,648,563-144,649,754 MROH6
    nsv4813888copy number variation1nstd200human GRCh37 chr8: 144,648,563-144,649,754 , GRCh38.p12 chr8: 143,566,393-143,567,584 , GRCh38.p12 chr8|NT_187571.1: 56,433-57,624 MROH6
    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
    nsv4676049copy number variation1nstd102humanPathogenic GRCh37 chr8: 143,616,831-144,930,611 , GRCh38.p12 chr8: 142,535,470-143,848,439 PYCR3, MROH4P, 69 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
    nsv4675029copy number variation1nstd102humanPathogenic GRCh37 chr8: 142,132,678-145,569,441 , GRCh38.p12 chr8: 141,122,579-144,345,779 RHPN1-AS1, MIR6847, 117 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
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4456783copy number variation1nstd102humanPathogenic GRCh37 chr8: 122,193,546-146,295,771 , GRCh38.p12 chr8: 121,181,306-145,070,385 HAS2, ZNF696, 369 more genes
    nsv4455524copy number variation1nstd102humanPathogenic GRCh37 chr8: 136,059,859-146,295,771 , GRCh38.p12 chr8: 135,047,616-145,070,385 LINC00051, LOC107986982, 197 more genes
    nsv4455260copy number variation1nstd102humanUncertain significance GRCh37 chr8: 144,190,206-146,295,771 , GRCh38.p12 chr8: 143,108,789-145,070,385 COMMD5, RHPN1-AS1, 113 more genes
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