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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4604607copy number variation1nstd183human GRCh37 chr8: 30,172,267-30,193,991 , GRCh38.p12 chr8: 30,314,751-30,336,475 LOC100128441
    nsv4457019copy number variation1nstd102humanUncertain significance GRCh37 chr8: 29,103,983-35,728,509 , GRCh38.p12 chr8: 29,246,466-35,870,991 TAGLN2P2, GSR, 87 more genes
    nsv4409310copy number variation1nstd174human GRCh37 chr8: 30,163,252-30,193,979 , GRCh38.p12 chr8: 30,305,736-30,336,463 LOC100128441
    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
    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
    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
    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
    nsv3923302copy number variation1nstd102humanPathogenic GRCh38 chr8: 24,910,364-31,210,737 , NCBI36 chr8: 24,823,781-31,187,795 , GRCh37 chr8: 24,767,877-31,068,253 BNIP3L, RNU6-178P, 123 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
    nsv3922931copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,383,584-36,370,018 , NCBI36 chr8: 12,285,464-36,347,088 , GRCh37 chr8: 12,241,093-36,227,536 LOC105379303, MTND2P32, 361 more genes
    nsv3921773copy number variation1nstd102humanPathogenic NCBI36 chr8: 12,511,855-43,310,472 , GRCh38 chr8: 12,609,975-43,336,172 , GRCh37 chr8: 12,467,484-43,191,315 RPL5P22, ZMAT4, 481 more genes
    nsv3921539copy number variation1nstd102humanPathogenic NCBI36 chr8: 153,682-47,058,107 , GRCh37.p13 chr8: 163,682-46,938,942 , GRCh38.p12 chr8: 213,682-46,027,320 HSPD1P3, RNA5SP253, 770 more genes
    nsv3921035copy number variation2nstd102humanPathogenic GRCh38 chr8: 12,728,904-43,673,207 , GRCh37 chr8: 12,586,413-43,528,350 , NCBI36 chr8: 12,630,784-43,647,507 MIR4287, RNU6-533P, 477 more genes
    nsv3920952copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,452-37,879,246 , GRCh38 chr8: 226,452-38,021,728 , NCBI36 chr8: 166,452-37,998,403 MTUS1, LINC00208, 666 more genes
    nsv3920259copy number variation1nstd102humanPathogenic GRCh38 chr8: 226,452-34,491,890 , GRCh37 chr8: 176,452-34,349,408 , NCBI36 chr8: 166,452-34,468,950 LOC100419761, LOC105377783, 624 more genes
    nsv3919926copy number variation1nstd102humanPathogenic GRCh37 chr8: 12,490,999-40,543,052 , GRCh38 chr8: 12,633,490-40,685,533 , NCBI36 chr8: 12,535,370-40,662,209 SH2D4A, BMP1, 423 more genes
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