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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148238copy number variation1nstd102humanPathogenic GRCh38 chr8: 115,586,904-135,607,135 , GRCh37.p13 chr8: 116,599,131-136,619,378 CCDC26, EFR3A, 238 more genes
    nsv7148132copy number variation1nstd102humanPathogenic GRCh37 chr8: 131,138,343-143,473,913 , GRCh38.p12 chr8: 130,126,097-142,392,552 LOC107983985, MIR30DHG, 104 more genes
    nsv7097893copy number variation1nstd102humanPathogenic GRCh37 chr8: 134,107,268-134,296,554 , GRCh38.p12 chr8: 133,095,024-133,284,311 SLA, TG, 4 more genes
    nsv7073939inversion1nstd229human GRCh38 chr8: 133,162,473-133,181,720 , GRCh37.p13 chr8: 134,174,717-134,193,964 LOC105375769
    nsv6853345copy number variation1nstd229human GRCh38 chr8: 133,142,551-133,153,951 , GRCh37.p13 chr8: 134,154,795-134,166,195 LOC105375769
    nsv6853085copy number variation1nstd229human GRCh38 chr8: 133,155,980-133,168,261 , GRCh37.p13 chr8: 134,168,224-134,180,505 LOC105375769
    nsv6850326copy number variation1nstd229human GRCh38 chr8: 133,154,968-133,161,532 , GRCh37.p13 chr8: 134,167,212-134,173,776 LOC105375769
    nsv6849804copy number variation1nstd229human GRCh38 chr8: 133,161,120-133,167,512 , GRCh37.p13 chr8: 134,173,364-134,179,756 LOC105375769
    nsv6844385copy number variation1nstd229human GRCh38 chr8: 132,809,731-133,525,064 , GRCh37.p13 chr8: 133,821,976-134,537,307 CCN4, ST13P6, 14 more genes
    nsv6844338copy number variation1nstd229human GRCh38 chr8: 133,153,701-133,168,300 , GRCh37.p13 chr8: 134,165,945-134,180,544 LOC105375769
    nsv6842863copy number variation1nstd229human GRCh38 chr8: 133,156,001-133,169,900 , GRCh37.p13 chr8: 134,168,245-134,182,144 LOC105375769
    nsv6841401copy number variation1nstd229human GRCh38 chr8: 133,010,316-136,879,429 , GRCh37.p13 chr8: 134,022,561-137,891,672 LOC107986978, LOC101927822, 35 more genes
    nsv6840303copy number variation1nstd229human GRCh38 chr8: 133,154,501-133,168,100 , GRCh37.p13 chr8: 134,166,745-134,180,344 LOC105375769
    nsv6839231copy number variation1nstd229human GRCh38 chr8: 133,158,336-133,170,750 , GRCh37.p13 chr8: 134,170,580-134,182,994 LOC105375769
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6574953inversion1nstd223human GRCh38 chr8: 133,162,473-133,181,721 , GRCh37.p13 chr8: 134,174,717-134,193,965 LOC105375769
    nsv6564870inversion1nstd223human GRCh38 chr8: 133,148,136-133,149,276 , GRCh37.p13 chr8: 134,160,380-134,161,520 LOC105375769
    nsv6432116copy number variation1nstd223human GRCh38 chr8: 133,026,354-133,228,293 , GRCh37.p13 chr8: 134,038,599-134,240,536 PTCSC1, LOC105375769, 5 more genes
    nsv6422625copy number variation1nstd223human GRCh38 chr8: 133,155,701-133,168,200 , GRCh37.p13 chr8: 134,167,945-134,180,444 LOC105375769
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
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