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Items: 1 to 20 of 135

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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
    nsv7093801copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,671,314-79,799,964 , GRCh38.p12 chr10: 73,911,556-78,040,206 COMTD1, DUSP13B, 53 more genes
    nsv7093731copy number variation1nstd102humanPathogenic GRCh37 chr10: 76,349,020-78,317,046 , GRCh38.p12 chr10: 74,589,262-76,557,288 ADK, SAMD8, 25 more genes
    nsv7063069inversion1nstd229human GRCh38 chr10: 75,019,895-76,543,360 , GRCh37.p13 chr10: 76,779,653-78,303,118 SAMD8, LOC105378367, 21 more genes
    nsv6895424copy number variation1nstd229human GRCh38 chr10: 75,720,464-75,720,873 , GRCh37.p13 chr10: 77,480,222-77,480,631 LRMDA, LOC105378367
    nsv6891080copy number variation1nstd229human GRCh38 chr10: 75,706,206-75,850,672 , GRCh37.p13 chr10: 77,465,964-77,610,430 LRMDA, LOC105378367
    nsv6890699copy number variation1nstd229human GRCh38 chr10: 75,721,351-75,724,526 , GRCh37.p13 chr10: 77,481,109-77,484,284 LRMDA, LOC105378367
    nsv6887374copy number variation1nstd229human GRCh38 chr10: 75,741,838-75,752,230 , GRCh37.p13 chr10: 77,501,596-77,511,988 LOC105378367, LRMDA
    nsv6885463copy number variation1nstd229human GRCh38 chr10: 75,736,047-75,738,902 , GRCh37.p13 chr10: 77,495,805-77,498,660 LOC105378367, LRMDA
    nsv6884489copy number variation1nstd229human GRCh38 chr10: 75,701,701-75,757,200 , GRCh37.p13 chr10: 77,461,459-77,516,958 LOC105378367, LRMDA
    nsv6882643copy number variation1nstd229human GRCh38 chr10: 75,723,903-75,724,526 , GRCh37.p13 chr10: 77,483,661-77,484,284 LRMDA, LOC105378367
    nsv6878846copy number variation1nstd229human GRCh38 chr10: 75,682,940-75,740,846 , GRCh37.p13 chr10: 77,442,698-77,500,604 LRMDA, LOC105378367
    nsv6314185copy number variation1nstd102humanPathogenic GRCh37 chr10: 68,735,254-78,885,714 , GRCh38.p12 chr10: 66,975,496-77,125,956 SLC25A16, CTNNA3, 204 more genes
    nsv6131808copy number variation1nstd213human GRCh37 chr10: 77,230,000-77,620,001 , GRCh38.p12 chr10: 75,470,242-75,860,243 LRMDA, MIR606, 1 more genes
    nsv5909992copy number variation1nstd209human GRCh38 chr10: 72,964,663-80,533,256 , GRCh37.p13 chr10: 74,724,421-82,293,012 , PRXL2A, 155 more genes
    nsv5481020copy number variation1nstd206human GRCh38 chr10: 75,736,695-75,742,611 , GRCh37.p13 chr10: 77,496,453-77,502,369 LOC105378367, LRMDA
    nsv5318597copy number variation1nstd204human GRCh37.p13 chr10: 77,463,611-77,477,429 , GRCh38.p13 chr10: 75,703,853-75,717,671 LRMDA, LOC105378367
    nsv5243324copy number variation1nstd204human GRCh38.p13 chr10: 75,705,053-75,717,427 , GRCh37.p13 chr10: 77,464,811-77,477,185 LRMDA, LOC105378367
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
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