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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098190copy number variation1nstd102humanUncertain significance GRCh37 chr8: 98,358,247-106,815,766 , GRCh38.p12 chr8: 97,346,019-105,803,538 RNU6-914P, RPL30, 159 more genes
    nsv7073952inversion1nstd229human GRCh38 chr8: 98,946,410-98,946,521 , GRCh37.p13 chr8: 99,958,638-99,958,749 OSR2
    nsv6857559copy number variation1nstd229human GRCh38 chr8: 98,789,708-99,000,924 , GRCh37.p13 chr8: 99,801,936-100,013,152 LOC643494, RN7SKP85, 6 more genes
    nsv6855857copy number variation1nstd229human GRCh38 chr8: 98,860,201-98,955,900 , GRCh37.p13 chr8: 99,872,429-99,968,128 OSR2, RN7SKP85, 5 more genes
    nsv6852303copy number variation1nstd229human GRCh38 chr8: 98,362,074-99,354,595 , GRCh37.p13 chr8: 99,374,302-100,366,823 MRPL57P7, LOC112268016, 16 more genes
    nsv6851827copy number variation1nstd229human GRCh38 chr8: 98,688,102-99,008,822 , GRCh37.p13 chr8: 99,700,330-100,021,050 LOC112268016, MRPL57P7, 7 more genes
    nsv6845562copy number variation1nstd229human GRCh38 chr8: 98,938,358-99,130,335 , GRCh37.p13 chr8: 99,950,586-100,142,563 LOC112268016, STK3, 4 more genes
    nsv6841189copy number variation1nstd229human GRCh38 chr8: 98,624,172-99,308,304 , GRCh37.p13 chr8: 99,636,400-100,320,532 LOC643494, LOC101928296, 10 more genes
    nsv6637706copy number variation1nstd102humanUncertain significance GRCh37 chr8: 99,132,556-100,021,840 , GRCh38.p12 chr8: 98,120,328-99,009,612 OSR2, KCNS2, 18 more genes
    nsv6637577copy number variation1nstd102humanUncertain significance GRCh37 chr8: 99,681,017-100,059,441 , GRCh38.p12 chr8: 98,668,789-99,047,213 LOC643494, RPL19P14, 8 more genes
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 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
    nsv6423758copy number variation1nstd223human GRCh38 chr8: 98,946,496-98,946,917 , GRCh37.p13 chr8: 99,958,724-99,959,145 OSR2
    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
    nsv6313658copy number variation1nstd102humanUncertain significance GRCh37 chr8: 99,834,003-100,199,851 , GRCh38.p12 chr8: 98,821,775-99,187,623 LOC643494, RN7SKP85, 7 more genes
    nsv6312925copy number variation1nstd102humanUncertain significance GRCh37 chr8: 99,135,566-100,205,305 , GRCh38.p12 chr8: 98,123,338-99,193,077 RNU6-914P, VPS13B, 19 more genes
    nsv6312665copy number variation1nstd102humanUncertain significance GRCh37 chr8: 99,135,566-106,815,766 , GRCh38.p12 chr8: 98,123,338-105,803,538 RNU6-748P, RN7SKP85, 144 more genes
    nsv6276236insertion1nstd214human GRCh38 chr8: 98,948,236-98,948,236 , GRCh37.p13 chr8: 99,960,464-99,960,464 OSR2
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