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Items: 1 to 20 of 203

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5705047mobile element insertion1nstd211human GRCh38 chr8: 33,493,643-33,493,643 , GRCh37.p13 chr8: 33,351,161-33,351,161 MAK16
    nsv5553736insertion1nstd206human GRCh38 chr8: 33,496,895-33,496,919 , GRCh37.p13 chr8: 33,354,413-33,354,437 MAK16, TTI2
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5111543mobile element insertion1nstd203human GRCh38 chr8: 33,495,468-33,495,484 , GRCh37.p13 chr8: 33,352,986-33,353,002 MAK16
    nsv4954317copy number variation1nstd200human GRCh38 chr8: 33,293,571-33,565,876 , GRCh37.p13 chr8: 33,151,089-33,423,394 TTI2, FUT10, 7 more genes
    nsv4769375copy number variation1nstd102humanUncertain significance GRCh37 chr8: 32,691,933-33,893,567 , GRCh38.p12 chr8: 32,834,415-34,036,049 SNORD13, BUD31P1, 21 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
    nsv4618574copy number variation1nstd183human GRCh37 chr8: 33,317,967-33,429,415 , GRCh38.p12 chr8: 33,460,449-33,571,897 RNF122, TTI2, 5 more genes
    nsv4614638copy number variation1nstd183human GRCh37 chr8: 33,151,920-33,423,070 , GRCh38.p12 chr8: 33,294,402-33,565,552 RNF122, TTI2, 7 more genes
    nsv4607890copy number variation1nstd183human GRCh37 chr8: 33,353,999-33,354,883 , GRCh38.p12 chr8: 33,496,481-33,497,365 TTI2, MAK16
    nsv4605998copy number variation1nstd183human GRCh37 chr8: 32,968,530-33,689,155 , GRCh38.p12 chr8: 33,111,012-33,831,637 , RNU6-528P, 14 more genes
    nsv4551479insertion1nstd166human GRCh37.p13 chr8: 33,354,413-33,354,413 , GRCh38.p12 chr8: 33,496,895-33,496,895 MAK16, TTI2
    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
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4368619copy number variation1nstd173human GRCh37 chr8: 33,317,982-33,345,243 , GRCh38.p12 chr8: 33,460,464-33,487,725 MAK16, FUT10
    nsv4368024copy number variation1nstd173human GRCh37 chr8: 33,314,623-33,345,243 , GRCh38.p12 chr8: 33,457,105-33,487,725 MAK16, FUT10
    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
    nsv4166466copy number variation1nstd166human GRCh37.p13 chr8: 33,353,275-33,500,585 , GRCh38.p12 chr8: 33,495,757-33,643,067 , BUD31P1, 8 more genes
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