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Items: 1 to 20 of 515

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 ENTPD4, LOC100421446, 447 more genes
    nsv7148146copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,721,809-30,183,737 , GRCh37.p13 chr8: 12,579,318-30,041,253 LOC101929028, RPL35P6, 274 more genes
    nsv7098732copy number variation1nstd102humanUncertain significance GRCh37 chr8: 17,915,043-20,112,692 , GRCh38.p12 chr8: 18,057,534-20,255,181 LOC107986868, ASAH1-AS1, 31 more genes
    nsv7074820inversion1nstd229human GRCh38 chr8: 17,929,527-19,508,705 , GRCh37.p13 chr8: 17,787,036-19,366,216 PSD3, LOC442382, 20 more genes
    nsv7071559inversion1nstd229human GRCh38 chr8: 15,858,861-19,517,388 , GRCh37.p13 chr8: 15,716,370-19,374,899 MTMR7, ADAM24P, 45 more genes
    nsv6857542copy number variation1nstd229human GRCh38 chr8: 18,998,582-19,578,893 , GRCh37.p13 chr8: 18,856,092-19,436,404 LOC105379306, LOC105379303, 7 more genes
    nsv6856996copy number variation1nstd229human GRCh38 chr8: 19,212,745-19,218,013 , GRCh37.p13 chr8: 19,070,255-19,075,523 LOC100128993
    nsv6856471copy number variation1nstd229human GRCh38 chr8: 19,224,501-19,231,800 , GRCh37.p13 chr8: 19,082,011-19,089,310 LOC100128993
    nsv6854703copy number variation1nstd229human GRCh38 chr8: 19,129,101-19,225,500 , GRCh37.p13 chr8: 18,986,611-19,083,010 LOC105379301, LOC100128993
    nsv6854337copy number variation1nstd229human GRCh38 chr8: 19,220,501-19,303,300 , GRCh37.p13 chr8: 19,078,011-19,160,811 LOC105379300, LOC100128993, 2 more genes
    nsv6854122copy number variation1nstd229human GRCh38 chr8: 19,210,724-19,676,197 , GRCh37.p13 chr8: 19,068,234-19,533,708 LOC442382, CSGALNACT1, 4 more genes
    nsv6853815copy number variation1nstd229human GRCh38 chr8: 19,041,670-19,378,002 , GRCh37.p13 chr8: 18,899,180-19,235,513 LOC105379301, LOC105379306, 5 more genes
    nsv6853516copy number variation1nstd229human GRCh38 chr8: 19,154,599-19,268,966 , GRCh37.p13 chr8: 19,012,109-19,126,476 LOC105379300, LOC100128993, 1 more genes
    nsv6852625copy number variation1nstd229human GRCh38 chr8: 18,974,797-19,484,133 , GRCh37.p13 chr8: 18,832,307-19,341,644 LOC105379300, LOC107986868, 8 more genes
    nsv6851359copy number variation1nstd229human GRCh38 chr8: 19,184,324-19,228,185 , GRCh37.p13 chr8: 19,041,834-19,085,695 LOC100128993
    nsv6851195copy number variation1nstd229human GRCh38 chr8: 18,689,206-19,227,195 , GRCh37.p13 chr8: 18,546,716-19,084,705 RPL35P6, LOC105379301, 4 more genes
    nsv6851052copy number variation1nstd229human GRCh38 chr8: 19,224,876-19,227,317 , GRCh37.p13 chr8: 19,082,386-19,084,827 LOC100128993
    nsv6847604copy number variation1nstd229human GRCh38 chr8: 19,191,551-19,245,373 , GRCh37.p13 chr8: 19,049,061-19,102,883 LOC105379300, LOC100128993, 1 more genes
    nsv6846433copy number variation1nstd229human GRCh38 chr8: 19,208,370-19,208,491 , GRCh37.p13 chr8: 19,065,880-19,066,001 LOC100128993
    nsv6846250copy number variation1nstd229human GRCh38 chr8: 19,226,589-19,226,785 , GRCh37.p13 chr8: 19,084,099-19,084,295 LOC100128993
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