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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
    nsv7097891copy number variation1nstd102humanUncertain significance GRCh37 chr8: 124,515,613-126,379,127 , GRCh38.p12 chr8: 123,503,373-125,366,885 FER1L6-AS1, LOC112268031, 35 more genes
    nsv7069598inversion1nstd229human GRCh38 chr8: 124,692,373-124,692,414 , GRCh37.p13 chr8: 125,704,614-125,704,655 MTSS1
    nsv6856523copy number variation1nstd229human GRCh38 chr8: 124,626,126-124,633,354 , GRCh37.p13 chr8: 125,638,367-125,645,595 MTSS1
    nsv6856090copy number variation1nstd229human GRCh38 chr8: 124,711,681-124,783,918 , GRCh37.p13 chr8: 125,723,922-125,796,160 MTSS1, LOC105375741
    nsv6856000copy number variation1nstd229human GRCh38 chr8: 124,373,188-128,390,224 , GRCh37.p13 chr8: 125,385,429-129,402,470 WASHC5, MIR4662B, 57 more genes
    nsv6854854copy number variation1nstd229human GRCh38 chr8: 124,417,443-124,594,587 , GRCh37.p13 chr8: 125,429,684-125,606,828 TRMT12, TATDN1, 6 more genes
    nsv6854694copy number variation1nstd229human GRCh38 chr8: 124,613,488-124,694,766 , GRCh37.p13 chr8: 125,625,729-125,707,007 MTSS1
    nsv6854251copy number variation1nstd229human GRCh38 chr8: 124,713,544-124,724,843 , GRCh37.p13 chr8: 125,725,785-125,737,084 MTSS1
    nsv6853662copy number variation1nstd229human GRCh38 chr8: 124,653,959-124,664,722 , GRCh37.p13 chr8: 125,666,200-125,676,963 MTSS1
    nsv6853419copy number variation1nstd229human GRCh38 chr8: 124,408,195-124,550,908 , GRCh37.p13 chr8: 125,420,436-125,563,149 TATDN1, MTSS1, 5 more genes
    nsv6853266copy number variation1nstd229human GRCh38 chr8: 124,631,075-124,635,445 , GRCh37.p13 chr8: 125,643,316-125,647,686 MTSS1
    nsv6853137copy number variation1nstd229human GRCh38 chr8: 124,668,356-124,668,909 , GRCh37.p13 chr8: 125,680,597-125,681,150 MTSS1
    nsv6850693copy number variation1nstd229human GRCh38 chr8: 124,603,264-124,607,905 , GRCh37.p13 chr8: 125,615,505-125,620,146 MTSS1
    nsv6849682copy number variation1nstd229human GRCh38 chr8: 124,714,491-124,718,627 , GRCh37.p13 chr8: 125,726,732-125,730,868 MTSS1
    nsv6844852copy number variation1nstd229human GRCh38 chr8: 124,689,167-124,689,331 , GRCh37.p13 chr8: 125,701,408-125,701,572 MTSS1
    nsv6844101copy number variation1nstd229human GRCh38 chr8: 124,550,073-124,550,376 , GRCh37.p13 chr8: 125,562,314-125,562,617 MTSS1, NDUFB9
    nsv6843139copy number variation1nstd229human GRCh38 chr8: 124,544,801-124,549,400 , GRCh37.p13 chr8: 125,557,042-125,561,641 MTSS1, NDUFB9
    nsv6842673copy number variation1nstd229human GRCh38 chr8: 124,689,089-124,692,608 , GRCh37.p13 chr8: 125,701,330-125,704,849 MTSS1
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