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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
    nsv7148124copy number variation1nstd102humanPathogenic GRCh37 chr8: 118,185,471-126,635,744 , GRCh38.p12 chr8: 117,173,232-125,623,500 LINC02964, TATDN1, 115 more genes
    nsv7141637insertion1nstd232human GRCh37.p13 chr8: 126,017,946-126,017,946 , GRCh38.p12 chr8: 125,005,704-125,005,704 SQLE
    nsv7138006copy number variation1nstd232human GRCh37.p13 chr8: 126,021,324-126,021,410 , GRCh38.p12 chr8: 125,009,082-125,009,168 SQLE
    nsv7097891copy number variation1nstd102humanUncertain significance GRCh37 chr8: 124,515,613-126,379,127 , GRCh38.p12 chr8: 123,503,373-125,366,885 FER1L6-AS1, LOC112268031, 35 more genes
    nsv7065632inversion1nstd229human GRCh38 chr8: 124,740,246-125,017,267 , GRCh37.p13 chr8: 125,752,488-126,029,509 MIR4662A, MIR4662B, 8 more genes
    nsv6856728copy number variation1nstd229human GRCh38 chr8: 125,019,279-125,019,487 , GRCh37.p13 chr8: 126,031,521-126,031,729 SQLE
    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
    nsv6851858copy number variation1nstd229human GRCh38 chr8: 124,810,518-125,324,458 , GRCh37.p13 chr8: 125,822,760-126,336,700 RN7SL329P, LOC105375742, 10 more genes
    nsv6849802copy number variation1nstd229human GRCh38 chr8: 124,998,173-124,998,226 , GRCh37.p13 chr8: 126,010,415-126,010,468 SQLE-DT, SQLE
    nsv6847310copy number variation1nstd229human GRCh38 chr8: 125,019,525-125,019,713 , GRCh37.p13 chr8: 126,031,767-126,031,955 SQLE
    nsv6846908copy number variation1nstd229human GRCh38 chr8: 124,997,941-125,002,510 , GRCh37.p13 chr8: 126,010,183-126,014,752 SQLE-DT, SQLE
    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
    nsv6575539inversion1nstd223human GRCh38 chr8: 125,008,101-125,009,809 , GRCh37.p13 chr8: 126,020,343-126,022,051 SQLE
    nsv6435315copy number variation1nstd223human GRCh38 chr8: 125,008,193-125,013,456 , GRCh37.p13 chr8: 126,020,435-126,025,698 SQLE
    nsv6428753copy number variation1nstd223human GRCh38 chr8: 125,019,276-125,019,487 , GRCh37.p13 chr8: 126,031,518-126,031,729 SQLE
    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
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