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Items: 1 to 20 of 293

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7077505inversion1nstd229human GRCh38 chr10: 17,905,883-17,905,917 , GRCh37.p13 chr10|NW_003315932.1: 334,674-334,708 MRC1
    nsv7074917inversion1nstd229human GRCh38 chr10: 17,830,863-17,830,898 , GRCh37.p13 chr10|NW_003315932.1: 259,654-259,689 MRC1
    nsv7072770inversion1nstd229human GRCh38 chr10: 17,877,710-17,877,782 , GRCh37.p13 chr10|NW_003315932.1: 306,501-306,573 MRC1
    nsv7072716inversion1nstd229human GRCh38 chr10: 17,803,406-17,856,179 , GRCh37.p13 chr10|NW_003315932.1: 232,197-284,970 MRC1, MIR511
    nsv7069569inversion1nstd229human GRCh38 chr10: 17,902,522-17,902,596 , GRCh37.p13 chr10|NW_003315932.1: 331,313-331,387 MRC1
    nsv7066269inversion1nstd229human GRCh38 chr10: 17,800,810-17,892,873 , GRCh37.p13 chr10|NW_003315932.1: 229,601-321,664 MRC1, MIR511, 1 more genes
    nsv6894655copy number variation1nstd229human GRCh38 chr10: 17,814,824-17,816,013 , GRCh37.p13 chr10|NW_003315932.1: 243,615-244,804 MRC1
    nsv6894195copy number variation1nstd229human GRCh38 chr10: 17,863,687-17,865,636 , GRCh37.p13 chr10|NW_003315932.1: 292,478-294,427 MRC1
    nsv6893059copy number variation1nstd229human GRCh38 chr10: 17,888,477-17,894,006 , GRCh37.p13 chr10|NW_003315932.1: 317,268-322,797 MRC1
    nsv6891877copy number variation1nstd229human GRCh38 chr10: 17,860,295-17,860,485 , GRCh37.p13 chr10|NW_003315932.1: 289,086-289,276 MRC1
    nsv6891805copy number variation1nstd229human GRCh38 chr10: 17,864,051-17,864,247 , GRCh37.p13 chr10|NW_003315932.1: 292,842-293,038 MRC1
    nsv6891205copy number variation1nstd229human GRCh38 chr10: 17,856,201-17,892,800 , GRCh37.p13 chr10|NW_003315932.1: 284,992-321,591 MRC1
    nsv6890945copy number variation1nstd229human GRCh38 chr10: 17,871,708-17,871,756 , GRCh37.p13 chr10|NW_003315932.1: 300,499-300,547 MRC1
    nsv6887258copy number variation1nstd229human GRCh38 chr10: 17,813,421-17,821,862 , GRCh37.p13 chr10|NW_003315932.1: 242,212-250,653 MRC1
    nsv6887030copy number variation1nstd229human GRCh38 chr10: 17,843,881-17,844,588 , GRCh37.p13 chr10|NW_003315932.1: 272,672-273,379 MRC1, MIR511
    nsv6886668copy number variation1nstd229human GRCh38 chr10: 17,607,297-18,187,851 , GRCh37.p13 chr10|NW_003315932.1: 36,088-392,792 , GRCh37.p13 chr10: 17,649,296-18,252,930 STAM, TMEM236, 7 more genes
    nsv6883800copy number variation1nstd229human GRCh38 chr10: 17,809,786-17,818,692 , GRCh37.p13 chr10|NW_003315932.1: 238,577-247,483 MRC1
    nsv6882178copy number variation1nstd229human GRCh38 chr10: 17,840,130-17,840,149 , GRCh37.p13 chr10|NW_003315932.1: 268,921-268,940 MRC1
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