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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148238copy number variation1nstd102humanPathogenic GRCh38 chr8: 115,586,904-135,607,135 , GRCh37.p13 chr8: 116,599,131-136,619,378 CCDC26, EFR3A, 238 more genes
    nsv7077533inversion1nstd229human GRCh38 chr8: 125,245,829-133,039,076 , GRCh37.p13 chr8: 126,258,071-134,051,321 PVT1, MTRF1LP2, 76 more genes
    nsv7059128inversion1nstd229human GRCh38 chr8: 125,606,752-126,514,963 , GRCh37.p13 chr8: 126,618,996-127,527,208 KNOP1P5, RFPL4AP5, 7 more genes
    nsv6856000copy number variation1nstd229human GRCh38 chr8: 124,373,188-128,390,224 , GRCh37.p13 chr8: 125,385,429-129,402,470 WASHC5, MIR4662B, 57 more genes
    nsv6845860copy number variation1nstd229human GRCh38 chr8: 125,942,919-125,949,045 , GRCh37.p13 chr8: 126,955,163-126,961,289 LINC00861
    nsv6637224copy number variation1nstd102humanPathogenic GRCh37 chr8: 112,234,557-133,668,379 , GRCh38.p12 chr8: 111,222,328-132,656,133 RNU4-37P, LOC100420215, 220 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
    nsv6314744copy number variation1nstd102humanPathogenic GRCh37 chr8: 96,496,503-146,295,711 , GRCh38.p12 chr8: 95,484,275-145,070,325 OSR2, LOC392268, 676 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6136309copy number variation1nstd213human GRCh37 chr8: 122,920,000-127,650,001 , GRCh38.p12 chr8: 121,907,761-126,637,756 TBC1D31, FAM91A1, 77 more genes
    nsv6136244copy number variation1nstd213human GRCh37 chr8: 126,770,000-127,000,001 , GRCh38.p12 chr8: 125,757,756-125,987,757 LINC00861, RNU6-442P
    nsv6136082copy number variation1nstd213human GRCh37 chr8: 86,730,000-142,740,001 , GRCh38.p12 chr8: 85,717,771-141,729,803 ANXA13, ATP6V1C1, 658 more genes
    nsv6135822copy number variation1nstd213human GRCh37 chr8: 124,520,000-127,320,001 , GRCh38.p12 chr8: 123,507,760-126,307,756 RNF139, LINC00964, 42 more genes
    nsv6001440copy number variation1nstd212human GRCh38 chr8: 125,920,628-125,920,706 , GRCh37.p13 chr8: 126,932,872-126,932,950 LINC00861
    nsv5914088copy number variation1nstd209human GRCh38 chr8: 125,933,731-125,939,314 , GRCh37.p13 chr8: 126,945,975-126,951,558 LINC00861
    nsv5853457copy number variation1nstd209human GRCh38 chr8: 125,933,892-125,939,310 , GRCh37.p13 chr8: 126,946,136-126,951,554 LINC00861
    nsv5480238copy number variation1nstd206human GRCh38 chr8: 125,933,735-125,939,315 , GRCh37.p13 chr8: 126,945,979-126,951,559 LINC00861
    nsv5379413translocation1nstd200human GRCh38 chr8: 125,932,252-125,932,252 , GRCh38 chr8: 125,932,331-125,932,331 , GRCh37.p13 chr8: 126,944,575-126,944,575 , GRCh37.p13 chr8: 126,944,496-126,944,496 LINC00861
    nsv5116912mobile element insertion1nstd203human GRCh38 chr8: 125,936,001-125,936,015 , GRCh37.p13 chr8: 126,948,245-126,948,259 LINC00861
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