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Items: 1 to 20 of 262

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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
    nsv7098159copy number variation1nstd102humanUncertain significance GRCh37 chr8: 124,545,411-125,559,374 , GRCh38.p12 chr8: 123,533,171-124,547,133 LOC105375738, LOC101927588, 20 more genes
    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
    nsv7077170inversion1nstd229human GRCh38 chr8: 123,527,411-123,532,163 , GRCh37.p13 chr8: 124,539,651-124,544,403 FBXO32
    nsv7077052inversion1nstd229human GRCh38 chr8: 122,556,885-123,611,669 , GRCh37.p13 chr8: 123,569,124-124,623,909 RNY4P5, ZHX2, 27 more genes
    nsv7062121inversion1nstd229human GRCh38 chr8: 123,505,027-123,662,170 , GRCh37.p13 chr8: 124,517,267-124,674,410 FBXO32, KLHL38, 2 more genes
    nsv6851647copy number variation1nstd229human GRCh38 chr8: 123,537,901-123,601,400 , GRCh37.p13 chr8: 124,550,141-124,613,640 FBXO32, RN7SKP155
    nsv6846578copy number variation1nstd229human GRCh38 chr8: 123,537,389-123,538,058 , GRCh37.p13 chr8: 124,549,629-124,550,298 FBXO32
    nsv6841885copy number variation1nstd229human GRCh38 chr8: 123,538,913-123,539,289 , GRCh37.p13 chr8: 124,551,153-124,551,529 FBXO32
    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
    nsv6567805inversion1nstd223human GRCh38 chr8: 123,519,366-123,519,961 , GRCh37.p13 chr8: 124,531,606-124,532,201 FBXO32
    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
    nsv6246613mobile element insertion1nstd215human GRCh38 chr8: 123,525,800-123,525,800 , GRCh37.p13 chr8: 124,538,040-124,538,040 FBXO32
    nsv6136311copy number variation1nstd213human GRCh37 chr8: 124,440,000-124,600,001 , GRCh38.p12 chr8: 123,427,760-123,587,761 NTAQ1, FBXO32, 1 more genes
    nsv6136310copy number variation1nstd213human GRCh37 chr8: 123,620,000-124,800,001 , GRCh38.p12 chr8: 122,607,761-123,787,761 TBC1D31, FAM91A1, 31 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
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