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Items: 1 to 20 of 122

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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
    nsv6881522copy number variation1nstd229human GRCh38 chr10: 73,631,239-73,631,610 , GRCh37.p13 chr10: 75,390,997-75,391,368 MYOZ1
    nsv6878820copy number variation1nstd229human GRCh38 chr10: 73,633,110-73,635,976 , GRCh37.p13 chr10: 75,392,868-75,395,734 MYOZ1
    nsv6878248copy number variation1nstd229human GRCh38 chr10: 73,631,978-73,632,349 , GRCh37.p13 chr10: 75,391,736-75,392,107 MYOZ1
    nsv6620678copy number variation1nstd224human GRCh37 chr10: 75,391,217-75,477,298 , GRCh38.p12 chr10: 73,631,459-73,717,540 MYOZ1, SYNPO2L, 5 more genes
    nsv6591215inversion1nstd223human GRCh38 chr10: 73,629,760-73,629,969 , GRCh37.p13 chr10: 75,389,518-75,389,727 MYOZ1
    nsv6454715copy number variation1nstd223human GRCh38 chr10: 73,626,842-73,630,422 , GRCh37.p13 chr10: 75,386,600-75,390,180 MYOZ1, USP54
    nsv6451819copy number variation1nstd223human GRCh38 chr10: 73,597,801-73,749,000 , GRCh37.p13 chr10: 75,357,559-75,508,758 GLUD1P3, BMS1P4, 9 more genes
    nsv6444761copy number variation1nstd223human GRCh38 chr10: 73,592,601-73,761,100 , GRCh37.p13 chr10: 75,352,359-75,520,858 SYNPO2L-AS1, SYNPO2L, 9 more genes
    nsv6441859copy number variation1nstd223human GRCh38 chr10: 73,595,801-73,749,100 , GRCh37.p13 chr10: 75,355,559-75,508,858 MYOZ1, BMS1P4-AGAP5, 9 more genes
    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
    nsv6132050copy number variation1nstd213human GRCh37 chr10: 75,330,000-75,750,001 , GRCh38.p12 chr10: 73,570,242-73,990,243 CAMK2G, GLUD1P3, 18 more genes
    nsv5927537copy number variation1nstd209human GRCh38 chr10: 73,638,875-73,639,015 , GRCh37.p13 chr10: 75,398,633-75,398,773 MYOZ1
    nsv5909992copy number variation1nstd209human GRCh38 chr10: 72,964,663-80,533,256 , GRCh37.p13 chr10: 74,724,421-82,293,012 , PRXL2A, 155 more genes
    nsv5708466mobile element insertion1nstd211human GRCh38 chr10: 73,640,568-73,640,568 , GRCh37.p13 chr10: 75,400,326-75,400,326 MYOZ1
    nsv5397923mobile element insertion1nstd206human GRCh38 chr10: 73,640,568-73,640,619 , GRCh37.p13 chr10: 75,400,326-75,400,377 MYOZ1
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4456093copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,251,395-75,763,287 , GRCh38.p12 chr10: 73,491,637-74,003,529 ZSWIM8-AS1, PPP3CB-AS1, 23 more genes
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
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