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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5248548copy number variation1nstd204human GRCh38.p13 chr8: 143,866,301-144,531,400 , GRCh37.p13 chr8: 145,146,063-145,756,784 MIR661, EXOSC4, 51 more genes
    nsv5105813mobile element insertion1nstd203human GRCh38 chr8: 144,525,937-144,525,949 , GRCh37.p13 chr8: 145,751,321-145,751,333 C8orf82, LRRC24
    nsv4962722copy number variation1nstd200human GRCh38 chr8: 144,517,146-144,522,246 , GRCh37.p13 chr8: 145,742,530-145,747,630 LRRC14, RECQL4, 1 more genes
    nsv4962721copy number variation1nstd200human GRCh38 chr8: 144,511,566-144,600,127 , GRCh37.p13 chr8: 145,736,949-145,825,511 RECQL4, LRRC14, 4 more genes
    nsv4813923copy number variation1nstd200human GRCh37 chr8: 145,742,530-145,747,630 , GRCh38.p12 chr8: 144,517,146-144,522,246 RECQL4, LRRC24, 1 more genes
    nsv4769373copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,033,244-146,297,937 , GRCh38.p12 chr8: 143,959,076-145,072,551 ZFTRAF1, PLEC, 68 more genes
    nsv4729603copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 144,262,042-146,295,771 , GRCh38.p12 chr8: 143,180,625-145,070,385 CYC1, EEF1D, 112 more genes
    nsv4729346copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,555,125-145,779,806 , GRCh38.p12 chr8: 144,331,462-144,554,422 FOXH1, MIR10400, 26 more genes
    nsv4675664copy number variation1nstd102humanPathogenic GRCh37 chr8: 128,877,995-146,295,771 , GRCh38.p12 chr8: 127,865,749-145,070,385 LOC105375789, LINC02990, 270 more genes
    nsv4675273copy number variation1nstd102humanPathogenic GRCh37 chr8: 121,042,467-146,295,771 , GRCh38.p12 chr8: 120,030,228-145,070,385 TOP1MT, SLA, 379 more genes
    nsv4609622copy number variation1nstd183human GRCh37 chr8: 145,744,429-145,904,090 , GRCh38.p12 chr8: 144,519,045-144,678,705 ARHGAP39, C8orf82, 2 more genes
    nsv4599460copy number variation1nstd183human GRCh37 chr8: 145,567,872-145,904,090 , GRCh38.p12 chr8: 144,344,210-144,678,705 RECQL4, ZFTRAF1, 25 more genes
    nsv4457078copy number variation1nstd102humanPathogenic GRCh37 chr8: 139,188,797-146,295,771 , GRCh38.p12 chr8: 138,176,554-145,070,385 GSDMD, MROH1, 181 more genes
    nsv4456997copy number variation1nstd102humanPathogenic GRCh37 chr8: 125,496,223-146,295,771 , GRCh38.p12 chr8: 124,483,982-145,070,385 LOC107986906, GPIHBP1, 317 more genes
    nsv4456942copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,695,493-145,798,535 , GRCh38.p12 chr8: 144,470,110-144,573,151 LOC101928953, KIFC2, 9 more genes
    nsv4456937copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,645,435-145,881,333 , GRCh38.p12 chr8: 144,431,464-144,655,948 LRRC14, RECQL4, 14 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
    nsv4456783copy number variation1nstd102humanPathogenic GRCh37 chr8: 122,193,546-146,295,771 , GRCh38.p12 chr8: 121,181,306-145,070,385 HAS2, ZNF696, 369 more genes
    nsv4455524copy number variation1nstd102humanPathogenic GRCh37 chr8: 136,059,859-146,295,771 , GRCh38.p12 chr8: 135,047,616-145,070,385 LINC00051, LOC107986982, 197 more genes
    nsv4455260copy number variation1nstd102humanUncertain significance GRCh37 chr8: 144,190,206-146,295,771 , GRCh38.p12 chr8: 143,108,789-145,070,385 COMMD5, RHPN1-AS1, 113 more genes
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