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Items: 1 to 20 of 253

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147823insertion1nstd232human GRCh37.p13 chr2: 62,096,690-62,096,690 , GRCh38.p12 chr2: 61,869,555-61,869,555 CCT4
    nsv7142517insertion1nstd232human GRCh37.p13 chr2: 62,099,726-62,099,726 , GRCh38.p12 chr2: 61,872,591-61,872,591 CCT4
    nsv7141667copy number variation1nstd232human GRCh37.p13 chr2: 62,100,247-62,100,330 , GRCh38.p12 chr2: 61,873,112-61,873,195 CCT4
    nsv7138974insertion1nstd232human GRCh37.p13 chr2: 62,099,452-62,099,452 , GRCh38.p12 chr2: 61,872,317-61,872,317 CCT4
    nsv7044192inversion1nstd229human GRCh38 chr2: 57,467,952-62,408,360 , GRCh37.p13 chr2: 57,695,087-62,635,495 RNA5SP94, PUS10, 62 more genes
    nsv6672280copy number variation1nstd229human GRCh38 chr2: 61,422,701-62,019,500 , GRCh37.p13 chr2: 61,649,836-62,246,635 LOC100422418, USP34, 13 more genes
    nsv6669775copy number variation1nstd229human GRCh38 chr2: 61,532,001-61,965,400 , GRCh37.p13 chr2: 61,759,136-62,192,535 XPO1, LOC100533678, 11 more genes
    nsv6669558copy number variation1nstd229human GRCh38 chr2: 61,875,621-61,875,781 , GRCh37.p13 chr2: 62,102,756-62,102,916 CCT4
    nsv6664318copy number variation1nstd229human GRCh38 chr2: 61,877,821-61,878,183 , GRCh37.p13 chr2: 62,104,956-62,105,318 CCT4
    nsv6663964copy number variation1nstd229human GRCh38 chr2: 61,872,615-61,872,927 , GRCh37.p13 chr2: 62,099,750-62,100,062 CCT4
    nsv6662167copy number variation1nstd229human GRCh38 chr2: 61,869,555-61,872,080 , GRCh37.p13 chr2: 62,096,690-62,099,215 CCT4
    nsv6658491copy number variation1nstd229human GRCh38 chr2: 61,652,215-61,888,506 , GRCh37.p13 chr2: 61,879,350-62,115,641 CCT4, LOC107985767, 7 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6628330copy number variation1nstd224human GRCh37 chr2: 61,916,221-62,094,945 , GRCh38.p12 chr2: 61,689,086-61,867,810 CCT4, FAM161A, 6 more genes
    nsv6544293inversion1nstd223human GRCh38 chr2: 61,873,862-61,874,453 , GRCh37.p13 chr2: 62,100,997-62,101,588 CCT4
    nsv6543888inversion1nstd223human GRCh38 chr2: 61,882,518-61,883,359 , GRCh37.p13 chr2: 62,109,653-62,110,494 CCT4
    nsv6352257copy number variation1nstd223human GRCh38 chr2: 61,881,453-61,882,291 , GRCh37.p13 chr2: 62,108,588-62,109,426 CCT4
    nsv6350753copy number variation1nstd223human GRCh38 chr2: 61,869,801-61,873,800 , GRCh37.p13 chr2: 62,096,936-62,100,935 CCT4
    nsv6350324copy number variation1nstd223human GRCh38 chr2: 61,845,877-61,973,371 , GRCh37.p13 chr2: 62,073,012-62,200,506 LOC100533678, COMMD1, 3 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
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