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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5642911insertion1nstd207human GRCh38 chr8: 144,071,290-144,071,290 , GRCh37.p13 chr8|NW_003315923.1: 409,937-409,937 , GRCh37.p13 chr8: 145,126,193-145,126,193 EXOSC4
    nsv5624944insertion1nstd207human GRCh38 chr8: 144,077,327-144,077,327 , GRCh37.p13 chr8: 145,132,230-145,132,230 , GRCh37.p13 chr8|NW_003315923.1: 415,974-415,974 EXOSC4
    nsv5489280copy number variation1nstd206human GRCh38 chr8: 144,071,263-144,071,321 , GRCh37.p13 chr8|NW_003315923.1: 409,910-409,968 , GRCh37.p13 chr8: 145,126,166-145,126,224 EXOSC4
    nsv5485823copy number variation1nstd206human GRCh38 chr8: 144,061,049-144,064,088 , GRCh37.p13 chr8|NW_003315923.1: 399,696-402,735 , GRCh37.p13 chr8: 145,115,952-145,118,991 EXOSC4, OPLAH
    nsv5381643copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,047,561-145,701,149 , GRCh38.p12 chr8: 143,973,393-144,475,766 ZFTRAF1, DGAT1, 40 more genes
    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
    nsv4962680copy number variation1nstd200human GRCh38 chr8: 144,066,287-144,075,442 , GRCh37.p13 chr8: 145,121,190-145,130,345 , GRCh37.p13 chr8|NW_003315923.1: 404,934-414,089 EXOSC4
    nsv4962677copy number variation1nstd200human GRCh38 chr8: 144,032,416-144,064,894 , GRCh37.p13 chr8|NW_003315923.1: 371,061-403,541 , GRCh37.p13 chr8: 145,091,963-145,119,797 OPLAH, SMPD5, 3 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
    nsv4743521copy number variation1nstd199human GRCh37 chr8: 145,126,057-145,126,159 , GRCh38.p12 chr8: 144,071,154-144,071,256 EXOSC4
    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
    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
    nsv4675029copy number variation1nstd102humanPathogenic GRCh37 chr8: 142,132,678-145,569,441 , GRCh38.p12 chr8: 141,122,579-144,345,779 RHPN1-AS1, MIR6847, 117 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
    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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