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Items: 1 to 20 of 269

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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
    nsv7148124copy number variation1nstd102humanPathogenic GRCh37 chr8: 118,185,471-126,635,744 , GRCh38.p12 chr8: 117,173,232-125,623,500 LINC02964, TATDN1, 115 more genes
    nsv7074087inversion1nstd229human GRCh38 chr8: 120,402,458-120,402,471 , GRCh37.p13 chr8: 121,414,697-121,414,710 MRPL13
    nsv7072142inversion1nstd229human GRCh38 chr8: 113,332,988-120,659,210 , GRCh37.p13 chr8: 114,345,217-121,671,450 ENPP2, RAD21-AS1, 67 more genes
    nsv6856831copy number variation1nstd229human GRCh38 chr8: 120,396,817-120,396,910 , GRCh37.p13 chr8: 121,409,056-121,409,149 MRPL13
    nsv6856245copy number variation1nstd229human GRCh38 chr8: 120,422,171-120,429,749 , GRCh37.p13 chr8: 121,434,411-121,441,989 MRPL13
    nsv6851051copy number variation1nstd229human GRCh38 chr8: 120,337,918-120,610,801 , GRCh37.p13 chr8: 121,350,157-121,623,041 SNTB1, MTBP, 2 more genes
    nsv6849927copy number variation1nstd229human GRCh38 chr8: 120,423,701-120,431,100 , GRCh37.p13 chr8: 121,435,941-121,443,340 MRPL13
    nsv6839019copy number variation1nstd229human GRCh38 chr8: 119,942,628-120,703,375 , GRCh37.p13 chr8: 120,954,868-121,715,615 MTBP, SNTB1, 5 more genes
    nsv6637672copy number variation1nstd102humanPathogenic GRCh37 chr8: 118,645,068-121,684,174 , GRCh38.p12 chr8: 117,632,829-120,671,934 RPS26P35, LOC105375723, 34 more genes
    nsv6637224copy number variation1nstd102humanPathogenic GRCh37 chr8: 112,234,557-133,668,379 , GRCh38.p12 chr8: 111,222,328-132,656,133 RNU4-37P, LOC100420215, 220 more genes
    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
    nsv6571119inversion1nstd223human GRCh38 chr8: 120,429,333-120,435,348 , GRCh37.p13 chr8: 121,441,573-121,447,588 MRPL13
    nsv6568927inversion1nstd223human GRCh38 chr8: 120,387,399-120,401,792 , GRCh37.p13 chr8: 121,399,638-121,414,031 MRPL13
    nsv6557805inversion1nstd223human GRCh38 chr8: 120,428,910-120,435,754 , GRCh37.p13 chr8: 121,441,150-121,447,994 MRPL13
    nsv6435445copy number variation1nstd223human GRCh38 chr8: 120,431,901-120,432,700 , GRCh37.p13 chr8: 121,444,141-121,444,940 MRPL13
    nsv6434580copy number variation1nstd223human GRCh38 chr8: 120,417,584-120,418,191 , GRCh37.p13 chr8: 121,429,824-121,430,431 MRPL13
    nsv6434289copy number variation1nstd223human GRCh38 chr8: 120,426,301-120,427,400 , GRCh37.p13 chr8: 121,438,541-121,439,640 MRPL13
    nsv6432027copy number variation1nstd223human GRCh38 chr8: 120,433,362-120,433,836 , GRCh37.p13 chr8: 121,445,602-121,446,076 MRPL13
    nsv6418076copy number variation1nstd223human GRCh38 chr8: 120,389,401-120,394,800 , GRCh37.p13 chr8: 121,401,640-121,407,039 MRPL13
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