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Items: 1 to 20 of 190

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5919722copy number variation1nstd209human GRCh38 chr8: 23,851,535-23,851,594 , GRCh37.p13 chr8: 23,709,048-23,709,107 STC1
    nsv5379155translocation1nstd200human GRCh38 chr8: 23,845,090-23,845,090 , GRCh38 chr8: 23,845,172-23,845,172 , GRCh37.p13 chr8: 23,702,685-23,702,685 , GRCh37.p13 chr8: 23,702,603-23,702,603 STC1
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
    nsv4756879inversion1nstd199human GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373 , ADRA1A, 411 more genes
    nsv4728911copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,528,482-29,886,483 , GRCh38.p12 chr8: 12,670,973-30,028,967 NAT1, NAT2, 272 more genes
    nsv4558223mobile element insertion1nstd166human GRCh37.p13 chr8: 23,706,979-23,706,979 , GRCh38.p12 chr8: 23,849,466-23,849,466 STC1
    nsv4526035copy number variation1nstd166human GRCh37.p13 chr8: 23,711,289-23,712,066 , GRCh38.p12 chr8: 23,853,776-23,854,553 STC1
    nsv4457159copy number variation1nstd102humanPathogenic GRCh37 chr8: 21,662,847-24,199,218 , GRCh38.p12 chr8: 21,805,335-24,341,705 SINHCAFP3, RPL23AP55, 66 more genes
    nsv4456504copy number variation1nstd102humanPathogenic GRCh37 chr8: 23,501,519-24,907,990 , GRCh38.p12 chr8: 23,644,006-25,050,475 RNU1-148P, LOC107986930, 19 more genes
    nsv4455606copy number variation1nstd102humanPathogenic GRCh37 chr8: 22,442,548-27,369,334 , GRCh38.p12 chr8: 22,585,035-27,511,817 PPP2R2A, LOC102723395, 91 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4348018copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,546,855-35,816,855 , GRCh38.p12 chr8: 12,689,346-35,959,337 NAT1, NAT2, 343 more genes
    nsv4166582copy number variation1nstd166human GRCh37.p13 chr8: 23,702,603-23,702,685 , GRCh38.p12 chr8: 23,845,090-23,845,172 STC1
    nsv3972390copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,556,004-34,374,150 , GRCh38.p12 chr8: 12,698,495-34,516,632 NAT1, NAT2, 335 more genes
    nsv3969454copy number variation1nstd168human GRCh38 chr8: 23,824,260-23,845,301 , GRCh37.p13 chr8: 23,681,773-23,702,814 STC1
    nsv3924532copy number variation1nstd102humanPathogenic NCBI36 chr8: 181,605-31,068,132 , GRCh38 chr8: 241,605-31,091,074 , GRCh37 chr8: 191,605-30,948,590 DEFB109B, GATA4, 585 more genes
    nsv3923600copy number variation1nstd102humanPathogenic NCBI36 chr8: 12,284,724-28,539,000 , GRCh37 chr8: 12,240,353-28,483,081 , GRCh38 chr8: 12,382,844-28,625,564 LOC105379340, LOC646708, 259 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
    nsv3923174copy number variation1nstd102humanPathogenic GRCh38 chr8: 18,972,996-33,619,264 , GRCh37 chr8: 18,830,506-33,476,782 , NCBI36 chr8: 18,874,786-33,596,324 RPLP1P9, CHRNA2, 259 more genes
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