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Items: 1 to 20 of 393

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137677copy number variation1nstd102humannot provided GRCh38 chr2: 47,804,639-48,361,567 , GRCh37.p13 chr2: 48,031,778-48,588,706 RNU4-49P, RN7SKP224, 11 more genes
    nsv5957014insertion1nstd209human GRCh38 chr2: 47,901,128-47,901,128 , GRCh37.p13 chr2: 48,128,267-48,128,267 FBXO11
    nsv5885606copy number variation1nstd209human GRCh38 chr2: 47,867,023-47,867,365 , GRCh37.p13 chr2: 48,094,162-48,094,504 FBXO11
    nsv5879074copy number variation1nstd209human GRCh38 chr2: 47,842,084-47,844,328 , GRCh37.p13 chr2: 48,069,223-48,071,467 FBXO11
    nsv5871025copy number variation1nstd209human GRCh38 chr2: 47,840,207-47,841,902 , GRCh37.p13 chr2: 48,067,346-48,069,041 FBXO11
    nsv5833368copy number variation1nstd209human GRCh38 chr2: 47,842,145-47,844,363 , GRCh37.p13 chr2: 48,069,284-48,071,502 FBXO11
    nsv5686861mobile element insertion1nstd211human GRCh38 chr2: 47,883,035-47,883,035 , GRCh37.p13 chr2: 48,110,174-48,110,174 RPS27AP7, FBXO11
    nsv5673706copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,635,530-48,035,526 , GRCh38.p12 chr2: 47,408,391-47,808,387 MSH6, MSH2, 7 more genes
    nsv5673624copy number variation1nstd102humanPathogenic GRCh37 chr2: 48,030,537-48,032,176 , GRCh38.p12 chr2: 47,803,398-47,805,037 MSH6, FBXO11
    nsv5673623copy number variation1nstd102humanPathogenic GRCh37 chr2: 48,023,023-48,033,800 , GRCh38.p12 chr2: 47,795,884-47,806,661 RPL36AP15, MSH6, 1 more genes
    nsv5673548copy number variation1nstd102humanPathogenic GRCh37 chr2: 48,010,211-48,033,885 , GRCh38.p12 chr2: 47,783,072-47,806,746 MSH6, FBXO11, 1 more genes
    nsv5673463copy number variation1nstd102humanPathogenic GRCh37 chr2: 48,025,740-48,032,937 , GRCh38.p12 chr2: 47,798,601-47,805,798 FBXO11, MSH6, 1 more genes
    nsv5673462copy number variation1nstd102humanPathogenic GRCh37 chr2: 48,025,740-48,032,572 , GRCh38.p12 chr2: 47,798,601-47,805,433 FBXO11, MSH6, 1 more genes
    nsv5673461copy number variation1nstd102humanPathogenic GRCh37 chr2: 48,023,027-48,032,172 , GRCh38.p12 chr2: 47,795,888-47,805,033 FBXO11, RPL36AP15, 1 more genes
    nsv5673460copy number variation1nstd102humanPathogenic GRCh37 chr2: 48,018,060-48,033,503 , GRCh38.p12 chr2: 47,790,921-47,806,364 FBXO11, RPL36AP15, 1 more genes
    nsv5673368copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 48,033,306-48,033,380 , GRCh38 chr2: 47,806,167-47,806,241 MSH6, FBXO11
    nsv5623029insertion1nstd207human GRCh38 chr2: 47,900,557-47,900,557 , GRCh37.p13 chr2: 48,127,696-48,127,696 FBXO11
    nsv5620680insertion1nstd207human GRCh38 chr2: 47,900,865-47,900,865 , GRCh37.p13 chr2: 48,128,004-48,128,004 FBXO11
    nsv5618555insertion1nstd207human GRCh38 chr2: 47,838,428-47,838,428 , GRCh37.p13 chr2: 48,065,567-48,065,567 FBXO11
    nsv5613695insertion1nstd207human GRCh38 chr2: 47,901,128-47,901,128 , GRCh37.p13 chr2: 48,128,267-48,128,267 FBXO11
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