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Items: 1 to 20 of 923

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139861copy number variation1nstd232human GRCh37.p13 chr21: 45,051,936-45,051,987 , GRCh38.p12 chr21: 43,632,055-43,632,106 HSF2BP
    nsv7096096copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr21: 43,160,998-47,754,702 , GRCh38.p12 chr21: 41,740,838-46,334,788 TSPEAR, LINC01424, 158 more genes
    nsv7076046inversion1nstd229human GRCh38 chr21: 42,633,367-44,550,173 , GRCh37.p13 chr21: 44,053,477-45,916,560 MYL6P1, MIR5692B, 68 more genes
    nsv7072799inversion1nstd229human GRCh38 chr21: 41,886,117-43,786,596 , GRCh37.p13 chr21: 43,306,226-45,206,477 ZNF295-AS1, LINC01668, 57 more genes
    nsv7064889inversion1nstd229human GRCh38 chr21: 41,632,756-44,900,321 , GRCh37.p13 chr21: 43,052,916-46,320,236 RNU6-1150P, LOC105372824, 123 more genes
    nsv7033340copy number variation1nstd229human GRCh38 chr21: 43,625,216-43,626,614 , GRCh37.p13 chr21: 45,045,097-45,046,495 HSF2BP
    nsv7032259copy number variation1nstd229human GRCh38 chr21: 43,599,778-43,610,897 , GRCh37.p13 chr21: 45,019,659-45,030,778 MIR6070, HSF2BP
    nsv7032059copy number variation1nstd229human GRCh38 chr21: 43,207,013-43,892,998 , GRCh37.p13 chr21: 44,627,123-45,312,879 RPL31P1, LINC03039, 19 more genes
    nsv7031048copy number variation1nstd229human GRCh38 chr21: 43,647,947-43,648,592 , GRCh37.p13 chr21: 45,067,828-45,068,473 HSF2BP
    nsv7030122copy number variation1nstd229human GRCh38 chr21: 43,625,577-43,630,960 , GRCh37.p13 chr21: 45,045,458-45,050,841 HSF2BP
    nsv7026531copy number variation1nstd229human GRCh38 chr21: 43,605,404-43,607,576 , GRCh37.p13 chr21: 45,025,285-45,027,457 HSF2BP
    nsv7023608copy number variation1nstd229human GRCh38 chr21: 43,594,665-43,595,472 , GRCh37.p13 chr21: 45,014,546-45,015,353 HSF2BP
    nsv7022421copy number variation1nstd229human GRCh38 chr21: 43,578,396-43,578,801 , GRCh37.p13 chr21: 44,998,277-44,998,682 HSF2BP
    nsv7021893copy number variation1nstd229human GRCh38 chr21: 43,620,298-43,623,746 , GRCh37.p13 chr21: 45,040,179-45,043,627 HSF2BP
    nsv7021630copy number variation1nstd229human GRCh38 chr21: 43,623,301-43,638,600 , GRCh37.p13 chr21: 45,043,182-45,058,481 HSF2BP
    nsv7019948copy number variation1nstd229human GRCh38 chr21: 40,558,832-43,971,067 , GRCh37.p13 chr21: 41,930,759-45,390,948 LOC105372821, PDXK, 86 more genes
    nsv7019432copy number variation1nstd229human GRCh38 chr21: 43,606,896-43,615,490 , GRCh37.p13 chr21: 45,026,777-45,035,371 HSF2BP, MIR6070
    nsv7018947copy number variation1nstd229human GRCh38 chr21: 43,582,567-43,588,121 , GRCh37.p13 chr21: 45,002,448-45,008,002 HSF2BP
    nsv6637459copy number variation1nstd102humanPathogenic GRCh37 chr21: 42,046,399-45,109,188 , GRCh38.p12 chr21: 40,674,473-43,689,307 LOC101928255, RRP1B, 74 more genes
    nsv6626624copy number variation1nstd224human GRCh37 chr21: 1-48,129,895 , GRCh38.p12 chr21: 8,522,361-46,699,983 , ATP5PO, 657 more genes
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