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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137049copy number variation1nstd102humanPathogenic GRCh37 chr6: 393,153-3,751,765 , GRCh38.p12 chr6: 393,153-3,751,531 LOC105374883, LINC02525, 57 more genes
    nsv7097820copy number variation1nstd102humanUncertain significance GRCh37 chr6: 3,104,439-3,157,697 , GRCh38.p12 chr6: 3,104,205-3,157,463 TUBB2A, RIPK1, 3 more genes
    nsv7097326copy number variation1nstd102humanUncertain significance GRCh37 chr6: 3,085,473-3,104,569 , GRCh38.p12 chr6: 3,085,239-3,104,335 RIPK1, RNA5SP201, 1 more genes
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7053151inversion1nstd229human GRCh38 chr6: 2,903,156-3,064,183 , GRCh37.p13 chr6: 2,903,390-3,064,417 SERPINB8P1, NQO2, 8 more genes
    nsv7047929inversion1nstd229human GRCh38 chr6: 2,249,577-5,332,355 , GRCh37.p13 chr6: 2,249,811-5,332,588 LOC107986561, NQO2-AS1, 67 more genes
    nsv7044205inversion1nstd229human GRCh38 chr6: 2,472,898-4,774,625 , GRCh37.p13 chr6: 2,473,132-4,774,859 TOMM5P1, PXDC1, 56 more genes
    nsv6796798copy number variation1nstd229human GRCh38 chr6: 3,071,176-3,071,419 , GRCh37.p13 chr6: 3,071,410-3,071,653 RIPK1
    nsv6795020copy number variation1nstd229human GRCh38 chr6: 3,070,995-3,074,056 , GRCh37.p13 chr6: 3,071,229-3,074,290 RIPK1
    nsv6788397copy number variation1nstd229human GRCh38 chr6: 3,070,369-3,072,597 , GRCh37.p13 chr6: 3,070,603-3,072,831 RIPK1
    nsv6785298copy number variation1nstd229human GRCh38 chr6: 2,759,301-4,105,800 , GRCh37.p13 chr6: 2,759,535-4,106,034 LOC107986557, SERPINB9-AS1, 39 more genes
    nsv6783949copy number variation1nstd229human GRCh38 chr6: 3,071,697-3,073,682 , GRCh37.p13 chr6: 3,071,931-3,073,916 RIPK1
    nsv6781472copy number variation1nstd229human GRCh38 chr6: 3,101,121-3,107,095 , GRCh37.p13 chr6: 3,101,355-3,107,329 LOC107986556, RIPK1
    nsv6636564copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,975-3,718,881 , GRCh38.p12 chr6: 156,975-3,718,647 LOC101927691, LOC107986555, 60 more genes
    nsv6574425inversion1nstd223human GRCh38 chr6: 3,100,182-3,100,751 , GRCh37.p13 chr6: 3,100,416-3,100,985 RIPK1
    nsv6568887inversion1nstd223human GRCh38 chr6: 2,903,210-3,064,173 , GRCh37.p13 chr6: 2,903,444-3,064,407 FAM136BP, LINC01011, 8 more genes
    nsv6413970copy number variation1nstd223human GRCh38 chr6: 3,079,139-3,081,513 , GRCh37.p13 chr6: 3,079,373-3,081,747 RIPK1
    nsv6404272copy number variation1nstd223human GRCh38 chr6: 3,071,697-3,073,681 , GRCh37.p13 chr6: 3,071,931-3,073,915 RIPK1
    nsv6402528copy number variation1nstd223human GRCh38 chr6: 3,069,469-3,069,876 , GRCh37.p13 chr6: 3,069,703-3,070,110 RIPK1
    nsv6400658copy number variation1nstd223human GRCh38 chr6: 2,956,035-3,081,695 , GRCh37.p13 chr6: 2,956,269-3,081,929 SERPINB6, FAM136BP, 7 more genes
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