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Items: 1 to 20 of 323

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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
    nsv7145956insertion1nstd232human GRCh37.p13 chr8: 124,262,560-124,262,560 , GRCh38.p12 chr8: 123,250,320-123,250,320 ZHX1, ZHX1-C8orf76
    nsv7077052inversion1nstd229human GRCh38 chr8: 122,556,885-123,611,669 , GRCh37.p13 chr8: 123,569,124-124,623,909 RNY4P5, ZHX2, 27 more genes
    nsv7064991inversion1nstd229human GRCh38 chr8: 122,266,535-123,404,204 , GRCh37.p13 chr8: 123,278,774-124,416,444 FAM83A, LOC107986904, 26 more genes
    nsv7064955inversion1nstd229human GRCh38 chr8: 123,228,574-123,244,112 , GRCh37.p13 chr8: 124,240,814-124,256,352 C8orf76, ZHX1-C8orf76, 1 more genes
    nsv7062653inversion1nstd229human GRCh38 chr8: 123,244,106-123,396,623 , GRCh37.p13 chr8: 124,256,346-124,408,863 RNU6-628P, MIR548AA1, 8 more genes
    nsv6857185copy number variation1nstd229human GRCh38 chr8: 123,259,200-123,260,116 , GRCh37.p13 chr8: 124,271,440-124,272,356 ZHX1, ZHX1-C8orf76
    nsv6850865copy number variation1nstd229human GRCh38 chr8: 123,139,571-123,226,289 , GRCh37.p13 chr8: 124,151,811-124,238,529 TBC1D31, TRM-CAT1-1, 5 more genes
    nsv6841331copy number variation1nstd229human GRCh38 chr8: 123,144,606-123,235,829 , GRCh37.p13 chr8: 124,156,846-124,248,069 C8orf76, UBA52P5, 6 more genes
    nsv6841135copy number variation1nstd229human GRCh38 chr8: 123,247,082-123,260,162 , GRCh37.p13 chr8: 124,259,322-124,272,402 ZHX1-C8orf76, ZHX1, 1 more genes
    nsv6838955copy number variation1nstd229human GRCh38 chr8: 123,259,256-123,380,191 , GRCh37.p13 chr8: 124,271,496-124,392,431 ZHX1-C8orf76, ZHX1, 7 more genes
    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
    nsv6575357inversion1nstd223human GRCh38 chr8: 123,264,831-123,264,988 , GRCh37.p13 chr8: 124,277,071-124,277,228 ZHX1, ZHX1-C8orf76
    nsv6572904inversion1nstd223human GRCh38 chr8: 123,267,736-123,268,621 , GRCh37.p13 chr8: 124,279,976-124,280,861 ZHX1, ZHX1-C8orf76
    nsv6563487inversion1nstd223human GRCh38 chr8: 123,268,009-123,268,505 , GRCh37.p13 chr8: 124,280,249-124,280,745 ZHX1-C8orf76, ZHX1
    nsv6563443inversion1nstd223human GRCh38 chr8: 123,256,769-123,256,955 , GRCh37.p13 chr8: 124,269,009-124,269,195 ZHX1, TRF-GAA12-1, 1 more genes
    nsv6559018inversion1nstd223human GRCh38 chr8: 123,233,303-123,233,411 , GRCh37.p13 chr8: 124,245,543-124,245,651 C8orf76, ZHX1-C8orf76
    nsv6431945copy number variation1nstd223human GRCh38 chr8: 123,248,101-123,250,000 , GRCh37.p13 chr8: 124,260,341-124,262,240 ZHX1, ZHX1-C8orf76
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