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Items: 1 to 20 of 236

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6114163mobile element insertion1nstd186human GRCh37 chr5: 9,627,495-9,627,546 , GRCh38.p12 chr5: 9,627,383-9,627,434 TAS2R1
    nsv5959327insertion1nstd209human GRCh38 chr5: 9,627,368-9,627,368 , GRCh37.p13 chr5: 9,627,480-9,627,480 TAS2R1
    nsv5843295copy number variation1nstd209human GRCh38 chr5: 9,623,273-9,625,372 , GRCh37.p13 chr5: 9,623,385-9,625,484 TAS2R1
    nsv5681034mobile element insertion2nstd211human GRCh38 chr5: 9,627,383-9,627,383 , GRCh37.p13 chr5: 9,627,495-9,627,495 TAS2R1
    nsv5394931mobile element insertion1nstd206human GRCh38 chr5: 9,627,383-9,627,434 , GRCh37.p13 chr5: 9,627,495-9,627,546 TAS2R1
    nsv5381771copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716 OTULINL, AKTIPP2, 317 more genes
    nsv5302377copy number variation1nstd204human GRCh38.p13 chr5: 9,513,102-9,991,247 , GRCh37.p13 chr5: 9,513,214-9,991,359 LINC02112, LOC101929359, 9 more genes
    nsv5231790copy number variation1nstd204human GRCh38.p13 chr5: 9,618,834-9,653,029 , GRCh37.p13 chr5: 9,618,946-9,653,141 LINC02112, TAS2R1
    nsv5226413copy number variation1nstd204human GRCh38.p13 chr5: 9,513,201-9,991,300 , GRCh37.p13 chr5: 9,513,313-9,991,412 TAS2R1, SNORD123, 9 more genes
    nsv5092009mobile element insertion1nstd203human GRCh38 chr5: 9,627,368-9,627,383 , GRCh37.p13 chr5: 9,627,480-9,627,495 TAS2R1
    nsv4944355copy number variation1nstd200human GRCh38 chr5: 9,319,071-9,756,451 , GRCh37.p13 chr5: 9,319,183-9,756,563 LINC02112, SNHG18, 6 more genes
    nsv4944354copy number variation1nstd200human GRCh38 chr5: 9,223,317-9,756,537 , GRCh37.p13 chr5: 9,223,429-9,756,649 TAS2R1, SNORD123, 6 more genes
    nsv4794889copy number variation1nstd200human GRCh37 chr5: 9,513,242-9,991,339 , GRCh38.p12 chr5: 9,513,130-9,991,227 LINC02112, RNA5SP177, 9 more genes
    nsv4794888copy number variation1nstd200human GRCh37 chr5: 9,319,183-9,756,563 , GRCh38.p12 chr5: 9,319,071-9,756,451 SNORD123, SEMA5A-AS1, 6 more genes
    nsv4794887copy number variation1nstd200human GRCh37 chr5: 9,223,429-9,756,649 , GRCh38.p12 chr5: 9,223,317-9,756,537 SEMA5A, SNORD123, 6 more genes
    nsv4725197insertion1nstd186human GRCh37 chr5: 9,627,480-9,627,480 , GRCh38.p12 chr5: 9,627,368-9,627,368 TAS2R1
    nsv4685752copy number variation1nstd102humanPathogenic GRCh37 chr5: 71,904-22,078,969 , GRCh38.p12 chr5: 71,789-22,078,860 LINC01377, LOC100421308, 277 more genes
    nsv4674497copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-14,738,180 , GRCh38.p12 chr5: 113,461-14,738,071 LOC101929003, MTCYBP37, 192 more genes
    nsv4674444copy number variation1nstd102humanPathogenic GRCh37 chr5: 1,322,680-10,762,544 , GRCh38.p12 chr5: 1,322,565-10,762,432 LOC100132773, LINC01019, 125 more genes
    nsv4674169copy number variation1nstd102humanUncertain significance GRCh37 chr5: 7,882,916-9,827,532 , GRCh38.p12 chr5: 7,882,803-9,827,420 LOC101929359, MTND6P2, 21 more genes
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