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Items: 1 to 20 of 234

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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
    nsv7093887copy number variation1nstd102humanUncertain significance GRCh37 chr10: 72,576,610-72,648,290 , GRCh38.p12 chr10: 70,816,854-70,888,533 SGPL1, PCBD1
    nsv7061849inversion1nstd229human GRCh38 chr10: 70,843,332-70,843,466 , GRCh37.p13 chr10: 72,603,089-72,603,223 SGPL1
    nsv6892303copy number variation1nstd229human GRCh38 chr10: 70,836,234-70,989,811 , GRCh37.p13 chr10: 72,595,991-72,749,568 LINC02622, PCBD1, 2 more genes
    nsv6889724copy number variation1nstd229human GRCh38 chr10: 70,819,177-70,821,755 , GRCh37.p13 chr10: 72,578,933-72,581,511 SGPL1
    nsv6888397copy number variation1nstd229human GRCh38 chr10: 70,843,680-70,843,846 , GRCh37.p13 chr10: 72,603,437-72,603,603 SGPL1
    nsv6885645copy number variation1nstd229human GRCh38 chr10: 70,835,902-70,839,674 , GRCh37.p13 chr10: 72,595,658-72,599,431 SGPL1
    nsv6885295copy number variation1nstd229human GRCh38 chr10: 70,860,557-70,866,709 , GRCh37.p13 chr10: 72,620,314-72,626,466 SGPL1
    nsv6884629copy number variation1nstd229human GRCh38 chr10: 70,839,255-70,843,004 , GRCh37.p13 chr10: 72,599,012-72,602,761 SGPL1
    nsv6882612copy number variation1nstd229human GRCh38 chr10: 70,881,215-70,881,611 , GRCh37.p13 chr10: 72,640,972-72,641,368 PCBD1, SGPL1
    nsv6880707copy number variation1nstd229human GRCh38 chr10: 70,831,157-70,831,206 , GRCh37.p13 chr10: 72,590,913-72,590,962 SGPL1
    nsv6620675copy number variation1nstd224human GRCh37 chr10: 72,012,813-73,062,048 , GRCh38.p12 chr10: 70,253,057-71,302,291 ADAMTS14, TBATA, 17 more genes
    nsv6620606copy number variation1nstd224human GRCh37 chr10: 72,109,893-72,996,234 , GRCh38.p12 chr10: 70,350,137-71,236,477 NODAL, PCBD1, 15 more genes
    nsv6451937copy number variation1nstd223human GRCh38 chr10: 70,841,201-70,843,000 , GRCh37.p13 chr10: 72,600,958-72,602,757 SGPL1
    nsv6450075copy number variation1nstd223human GRCh38 chr10: 70,855,701-70,865,500 , GRCh37.p13 chr10: 72,615,458-72,625,257 SGPL1
    nsv6445000copy number variation1nstd223human GRCh38 chr10: 70,819,177-70,821,751 , GRCh37.p13 chr10: 72,578,933-72,581,507 SGPL1
    nsv6444872copy number variation1nstd223human GRCh38 chr10: 70,293,423-70,921,060 , GRCh37.p13 chr10: 72,053,179-72,680,817 PALD1, YY1P1, 10 more genes
    nsv6436965copy number variation1nstd223human GRCh38 chr10: 70,839,255-70,843,001 , GRCh37.p13 chr10: 72,599,012-72,602,758 SGPL1
    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
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