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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148132copy number variation1nstd102humanPathogenic GRCh37 chr8: 131,138,343-143,473,913 , GRCh38.p12 chr8: 130,126,097-142,392,552 LOC107983985, MIR30DHG, 104 more genes
    nsv7076080inversion1nstd229human GRCh38 chr8: 137,223,456-143,780,837 , GRCh37.p13 chr8: 138,235,699-144,743,525 LOC107986906, FAM83H, 108 more genes
    nsv7061615inversion1nstd229human GRCh38 chr8: 139,238,401-143,070,465 , GRCh37.p13 chr8: 140,250,644-144,151,882 PEG13, LINC01300, 63 more genes
    nsv6868435copy number variation1nstd229human GRCh38 chr8: 141,962,196-142,061,605 , GRCh37.p13 chr8: 143,043,557-143,142,966 DNAJC8P3
    nsv6866096copy number variation1nstd229human GRCh38 chr8: 141,685,326-142,159,300 , GRCh37.p13 chr8: 142,695,426-143,240,661 DNAJC8P3, MIR1302-7
    nsv6865025copy number variation1nstd229human GRCh38 chr8: 141,929,673-141,966,185 , GRCh37.p13 chr8: 143,011,034-143,047,546 DNAJC8P3
    nsv6861932copy number variation1nstd229human GRCh38 chr8: 141,966,201-142,462,600 , GRCh37.p13 chr8: 143,047,562-143,543,961 LOC105375792, LINC00051, 5 more genes
    nsv6637926copy number variation1nstd102humanUncertain significance GRCh37 chr8: 142,309,348-143,247,742 , GRCh38.p12 chr8: 141,299,249-142,166,381 HNRNPA1P38, LOC105375791, 11 more genes
    nsv6637631copy number variation1nstd102humanUncertain significance GRCh37 chr8: 142,836,592-144,175,046 , GRCh38.p12 chr8: 141,755,231-143,093,629 CYP11B1, LOC105375792, 33 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
    nsv6632679copy number variation1nstd224human GRCh37 chr8: 142,937,043-143,284,328 , GRCh38.p12 chr8: 141,855,682-142,202,967 LINC00051, MIR4472-1, 2 more genes
    nsv6429369copy number variation1nstd223human GRCh38 chr8: 141,944,170-142,173,585 , GRCh37.p13 chr8: 143,025,531-143,254,946 DNAJC8P3
    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
    nsv6313513copy number variation1nstd102humanUncertain significance GRCh37 chr8: 142,326,501-143,237,710 , GRCh38.p12 chr8: 141,316,402-142,156,349 PTP4A3, LOC105375789, 10 more genes
    nsv6313487copy number variation1nstd102humanPathogenic GRCh37 chr8: 130,863,093-146,295,771 , GRCh38.p12 chr8: 129,850,847-145,070,385 LOC105375784, CYP11B2, 253 more genes
    nsv6136341copy number variation1nstd213human GRCh37 chr8: 142,830,000-144,520,001 , GRCh38.p12 chr8: 141,748,639-143,437,831 PSCA, ZC3H3, 48 more genes
    nsv6104087inversion1nstd212human GRCh38 chr8: 141,779,535-142,255,310 , GRCh37.p13 chr8: 142,860,896-143,336,671 , TSNARE1, 6 more genes
    nsv6008756copy number variation1nstd212human GRCh38 chr8: 141,658,448-142,255,360 , GRCh37.p13 chr8: 142,668,548-143,336,721 , TSNARE1, 6 more genes
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