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Items: 1 to 20 of 337

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 ENTPD4, LOC100421446, 447 more genes
    nsv7148146copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,721,809-30,183,737 , GRCh37.p13 chr8: 12,579,318-30,041,253 LOC101929028, RPL35P6, 274 more genes
    nsv7098732copy number variation1nstd102humanUncertain significance GRCh37 chr8: 17,915,043-20,112,692 , GRCh38.p12 chr8: 18,057,534-20,255,181 LOC107986868, ASAH1-AS1, 31 more genes
    nsv7097791copy number variation1nstd102humanUncertain significance GRCh37 chr8: 17,933,030-17,941,567 , GRCh38.p12 chr8: 18,075,521-18,084,058 ASAH1, ASAH1-AS1
    nsv7097790copy number variation1nstd102humanUncertain significance GRCh37 chr8: 17,924,709-17,941,567 , GRCh38.p12 chr8: 18,067,200-18,084,058 ASAH1, ASAH1-AS1
    nsv7074820inversion1nstd229human GRCh38 chr8: 17,929,527-19,508,705 , GRCh37.p13 chr8: 17,787,036-19,366,216 PSD3, LOC442382, 20 more genes
    nsv7071559inversion1nstd229human GRCh38 chr8: 15,858,861-19,517,388 , GRCh37.p13 chr8: 15,716,370-19,374,899 MTMR7, ADAM24P, 45 more genes
    nsv6857062copy number variation1nstd229human GRCh38 chr8: 18,012,123-18,117,346 , GRCh37.p13 chr8: 17,869,632-17,974,855 MRPS18CP3, PCM1, 3 more genes
    nsv6856041copy number variation1nstd229human GRCh38 chr8: 18,067,106-18,067,137 , GRCh37.p13 chr8: 17,924,615-17,924,646 ASAH1
    nsv6852437copy number variation1nstd229human GRCh38 chr8: 18,070,808-18,280,897 , GRCh37.p13 chr8: 17,928,317-18,138,406 MRPS18CP3, TRK-TTT17-1, 5 more genes
    nsv6851811copy number variation1nstd229human GRCh38 chr8: 17,666,115-18,117,017 , GRCh37.p13 chr8: 17,523,624-17,974,526 ASAH1, MIR548V, 8 more genes
    nsv6851171copy number variation1nstd229human GRCh38 chr8: 18,078,460-18,081,779 , GRCh37.p13 chr8: 17,935,969-17,939,288 ASAH1
    nsv6850159copy number variation1nstd229human GRCh38 chr8: 18,053,620-18,057,123 , GRCh37.p13 chr8: 17,911,129-17,914,632 ASAH1
    nsv6847692copy number variation1nstd229human GRCh38 chr8: 18,079,425-18,087,873 , GRCh37.p13 chr8: 17,936,934-17,945,382 ASAH1, ASAH1-AS1, 2 more genes
    nsv6844580copy number variation1nstd229human GRCh38 chr8: 17,879,610-18,681,214 , GRCh37.p13 chr8: 17,737,119-18,538,724 ABRAXAS1P2, RPL10AP11, 11 more genes
    nsv6840519copy number variation1nstd229human GRCh38 chr8: 18,059,086-18,283,362 , GRCh37.p13 chr8: 17,916,595-18,140,871 MRPS18CP3, TRK-TTT17-1, 5 more genes
    nsv6839436copy number variation1nstd229human GRCh38 chr8: 17,535,007-18,607,759 , GRCh37.p13 chr8: 17,392,516-18,465,269 MTUS1, LOC107986919, 18 more genes
    nsv6838702copy number variation1nstd229human GRCh38 chr8: 18,063,256-18,104,805 , GRCh37.p13 chr8: 17,920,765-17,962,314 MRPS18CP3, ASAH1, 2 more genes
    nsv6636968copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,049-18,936,715 , GRCh38.p12 chr8: 208,049-19,079,205 ZNF705B, NATP, 357 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
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