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Items: 1 to 20 of 423

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148204copy number variation1nstd102humanPathogenic GRCh38 chr5: 9,999-14,320,000 , GRCh37.p13 chr5: 10,001-14,320,109 LOC105379638, LOC100420683, 185 more genes
    nsv7099279copy number variation1nstd231human GRCh37 chr5: 1,810,638-3,031,002 , GRCh38.p12 chr5: 1,810,524-3,030,888 NDUFS6, IRX4, 12 more genes
    nsv7099278copy number variation1nstd231human GRCh37 chr5: 1,804,766-3,031,002 , GRCh38.p12 chr5: 1,804,652-3,030,888 NDUFS6, IRX4, 12 more genes
    nsv7099277copy number variation2nstd231human GRCh37 chr5: 1,804,766-3,030,981 , GRCh38.p12 chr5: 1,804,652-3,030,867 NDUFS6, IRX4, 12 more genes
    nsv7099276copy number variation1nstd231human GRCh37 chr5: 1,804,766-3,028,812 , GRCh38.p12 chr5: 1,804,652-3,028,698 NDUFS6, IRX4, 12 more genes
    nsv7045223inversion1nstd229human GRCh38 chr5: 2,721,510-7,652,208 , GRCh37.p13 chr5: 2,721,624-7,652,321 LOC105374620, LOC105374634, 60 more genes
    nsv7044124inversion1nstd229human GRCh38 chr5: 2,302,144-2,718,334 , GRCh37.p13 chr5: 2,302,258-2,718,448 LOC100506858, LSINCT5, 1 more genes
    nsv6771832copy number variation1nstd229human GRCh38 chr5: 2,738,801-2,741,300 , GRCh37.p13 chr5: 2,738,915-2,741,414 IRX2
    nsv6771620copy number variation1nstd229human GRCh38 chr5: 2,616,116-2,817,820 , GRCh37.p13 chr5: 2,616,230-2,817,934 IRX2-DT, LOC100130748, 2 more genes
    nsv6769791copy number variation1nstd229human GRCh38 chr5: 2,749,401-2,751,300 , GRCh37.p13 chr5: 2,749,515-2,751,414 IRX2-DT, IRX2
    nsv6769317copy number variation1nstd229human GRCh38 chr5: 2,712,602-2,715,236 , GRCh37.p13 chr5: 2,712,716-2,715,350 LSINCT5, IRX2
    nsv6768841copy number variation1nstd229human GRCh38 chr5: 2,735,201-2,751,400 , GRCh37.p13 chr5: 2,735,315-2,751,514 IRX2, IRX2-DT
    nsv6765506copy number variation1nstd229human GRCh38 chr5: 2,698,953-2,740,265 , GRCh37.p13 chr5: 2,699,067-2,740,379 LSINCT5, IRX2
    nsv6763480copy number variation1nstd229human GRCh38 chr5: 2,732,944-2,733,094 , GRCh37.p13 chr5: 2,733,058-2,733,208 IRX2
    nsv6763089copy number variation1nstd229human GRCh38 chr5: 2,709,721-2,719,153 , GRCh37.p13 chr5: 2,709,835-2,719,267 LSINCT5, IRX2
    nsv6762035copy number variation1nstd229human GRCh38 chr5: 2,696,200-2,713,039 , GRCh37.p13 chr5: 2,696,314-2,713,153 LSINCT5, IRX2
    nsv6758649copy number variation1nstd229human GRCh38 chr5: 1,642,551-2,905,290 , GRCh37.p13 chr5: 1,642,666-2,905,404 LOC105374618, LOC100506858, 13 more genes
    nsv6758109copy number variation1nstd229human GRCh38 chr5: 2,712,464-2,739,646 , GRCh37.p13 chr5: 2,712,578-2,739,760 IRX2, LSINCT5
    nsv6636942copy number variation1nstd102humanPathogenic GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932 LOC105374608, LSP1P3, 351 more genes
    nsv6636849copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-17,654,787 , GRCh38.p12 chr5: 113,462-17,654,678 ADCY2, HMGB3P3, 248 more genes
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