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Items: 1 to 20 of 285

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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
    nsv6889936copy number variation1nstd229human GRCh38 chr10: 68,936,251-68,936,351 , GRCh37.p13 chr10: 70,696,007-70,696,107 DDX50
    nsv6886419copy number variation1nstd229human GRCh38 chr10: 68,920,381-68,923,010 , GRCh37.p13 chr10: 70,680,137-70,682,766 DDX50
    nsv6884826copy number variation1nstd229human GRCh38 chr10: 68,886,307-68,928,869 , GRCh37.p13 chr10: 70,646,063-70,688,625 RNU6-571P, DDX50, 1 more genes
    nsv6588350inversion1nstd223human GRCh38 chr10: 68,909,645-68,910,186 , GRCh37.p13 chr10: 70,669,401-70,669,942 RNU6-571P, DDX50
    nsv6585345inversion1nstd223human GRCh38 chr10: 68,925,277-68,926,023 , GRCh37.p13 chr10: 70,685,033-70,685,779 DDX50
    nsv6584278inversion1nstd223human GRCh38 chr10: 68,915,528-68,918,126 , GRCh37.p13 chr10: 70,675,284-70,677,882 DDX50
    nsv6583815inversion1nstd223human GRCh38 chr10: 68,925,118-68,925,997 , GRCh37.p13 chr10: 70,684,874-70,685,753 DDX50
    nsv6577703inversion1nstd223human GRCh38 chr10: 68,908,424-68,908,613 , GRCh37.p13 chr10: 70,668,180-70,668,369 DDX50
    nsv6452788copy number variation1nstd223human GRCh38 chr10: 68,953,949-68,955,492 , GRCh37.p13 chr10: 70,713,705-70,715,248 DDX21, DDX50
    nsv6445744copy number variation1nstd223human GRCh38 chr10: 68,896,575-68,942,756 , GRCh37.p13 chr10: 70,656,331-70,702,512 DDX50, RNU6-571P
    nsv6441136copy number variation1nstd223human GRCh38 chr10: 68,951,459-68,953,565 , GRCh37.p13 chr10: 70,711,215-70,713,321 DDX50
    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
    nsv6308916copy number variation1nstd102humanUncertain significance GRCh37 chr10: 67,680,088-71,332,799 , GRCh38.p12 chr10: 65,920,330-69,573,043 RPS3AP38, MIR7151, 62 more genes
    nsv6173169copy number variation1nstd214human GRCh38 chr10: 68,936,251-68,936,350 , GRCh37.p13 chr10: 70,696,007-70,696,106 DDX50
    nsv6131968copy number variation1nstd213human GRCh37 chr10: 70,290,000-70,900,001 , GRCh38.p12 chr10: 68,530,243-69,140,245 DDX21, KIFBP, 15 more genes
    nsv6087409insertion1nstd212human GRCh38 chr10: 68,926,154-68,926,154 , GRCh37.p13 chr10: 70,685,910-70,685,910 DDX50
    nsv6011576copy number variation1nstd212human GRCh38 chr10: 68,926,070-68,926,173 , GRCh37.p13 chr10: 70,685,826-70,685,929 DDX50
    nsv5950301insertion1nstd209human GRCh38 chr10: 68,926,144-68,926,144 , GRCh37.p13 chr10: 70,685,900-70,685,900 DDX50
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