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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146183copy number variation1nstd232human GRCh37.p13 chr10: 14,750,858-14,750,922 , GRCh38.p12 chr10: 14,708,859-14,708,923 FAM107B
    nsv7142389copy number variation1nstd232human GRCh37.p13 chr10: 14,750,899-14,750,956 , GRCh38.p12 chr10: 14,708,900-14,708,957 FAM107B
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7073282inversion1nstd229human GRCh38 chr10: 12,099,288-14,830,781 , GRCh37.p13 chr10: 12,141,287-14,872,780 MIR1265, RNA5SP301, 45 more genes
    nsv7066219inversion1nstd229human GRCh38 chr10: 14,671,545-14,737,664 , GRCh37.p13 chr10: 14,713,544-14,779,663 FAM107B, RPSAP7
    nsv7061969inversion1nstd229human GRCh38 chr10: 11,128,019-14,526,691 , GRCh37.p13 chr10: 11,169,982-14,568,690 RPL5P25, LOC105376425, 58 more genes
    nsv7060184inversion1nstd229human GRCh38 chr10: 13,148,010-16,128,795 , GRCh37.p13 chr10: 13,190,010-16,170,794 LOC101928453, MCM10, 52 more genes
    nsv7058936inversion1nstd229human GRCh38 chr10: 14,706,807-14,710,198 , GRCh37.p13 chr10: 14,748,806-14,752,197 FAM107B
    nsv6896781copy number variation1nstd229human GRCh38 chr10: 14,732,601-14,733,200 , GRCh37.p13 chr10: 14,774,600-14,775,199 FAM107B
    nsv6896514copy number variation1nstd229human GRCh38 chr10: 14,749,444-14,751,145 , GRCh37.p13 chr10: 14,791,443-14,793,144 FAM107B
    nsv6896392copy number variation1nstd229human GRCh38 chr10: 14,605,409-14,612,962 , GRCh37.p13 chr10: 14,647,408-14,654,961 FAM107B
    nsv6895418copy number variation1nstd229human GRCh38 chr10: 14,574,373-14,579,711 , GRCh37.p13 chr10: 14,616,372-14,621,710 FAM107B
    nsv6894951copy number variation1nstd229human GRCh38 chr10: 14,762,318-14,773,135 , GRCh37.p13 chr10: 14,804,317-14,815,134 FAM107B
    nsv6894357copy number variation1nstd229human GRCh38 chr10: 14,763,671-14,764,070 , GRCh37.p13 chr10: 14,805,670-14,806,069 FAM107B
    nsv6894205copy number variation1nstd229human GRCh38 chr10: 14,632,765-14,632,808 , GRCh37.p13 chr10: 14,674,764-14,674,807 FAM107B
    nsv6894021copy number variation1nstd229human GRCh38 chr10: 14,522,665-14,525,685 , GRCh37.p13 chr10: 14,564,664-14,567,684 FAM107B
    nsv6893850copy number variation1nstd229human GRCh38 chr10: 14,710,881-14,714,299 , GRCh37.p13 chr10: 14,752,880-14,756,298 FAM107B
    nsv6893492copy number variation1nstd229human GRCh38 chr10: 14,709,533-14,717,150 , GRCh37.p13 chr10: 14,751,532-14,759,149 FAM107B
    nsv6892659copy number variation1nstd229human GRCh38 chr10: 14,587,147-14,587,215 , GRCh37.p13 chr10: 14,629,146-14,629,214 FAM107B
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