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Items: 1 to 20 of 237

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142384copy number variation1nstd232human GRCh37.p13 chr2: 26,414,263-26,414,349 , GRCh38.p12 chr2: 26,191,394-26,191,480 HADHA, GAREM2
    nsv7136951copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 26,467,859-26,486,247 , GRCh38.p12 chr2: 26,244,991-26,263,379 HADHA, HADHB
    nsv7096644copy number variation1nstd102humanPathogenic GRCh37 chr2: 26,416,426-26,418,121 , GRCh38.p12 chr2: 26,193,557-26,195,252 GAREM2, HADHA
    nsv7096643copy number variation1nstd102humanUncertain significance GRCh37 chr2: 26,414,119-26,712,628 , GRCh38.p12 chr2: 26,191,250-26,489,760 HADHA, ADGRF3, 6 more genes
    nsv7096625copy number variation1nstd102humanUncertain significance GRCh37 chr2: 24,443,763-30,143,525 , GRCh38.p12 chr2: 24,220,894-29,920,659 LOC105374381, POMC, 136 more genes
    nsv7096490copy number variation1nstd102humanPathogenic GRCh37 chr2: 26,414,119-26,462,031 , GRCh38.p12 chr2: 26,191,250-26,239,163 GAREM2, HADHA
    nsv7096150copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 26,455,008-26,457,243 , GRCh38.p12 chr2: 26,232,140-26,234,375 HADHA
    nsv7096148copy number variation2nstd102humanUncertain significance GRCh37 chr2: 24,443,763-29,022,169 , GRCh38.p12 chr2: 24,220,894-28,799,303 LOC105374381, SLC35F6, 122 more genes
    nsv6677384copy number variation1nstd229human GRCh38 chr2: 26,191,910-26,196,542 , GRCh37.p13 chr2: 26,414,779-26,419,411 GAREM2, HADHA
    nsv6677276copy number variation1nstd229human GRCh38 chr2: 26,221,900-26,239,826 , GRCh37.p13 chr2: 26,444,768-26,462,694 HADHA
    nsv6675982copy number variation1nstd229human GRCh38 chr2: 26,188,862-26,190,418 , GRCh37.p13 chr2: 26,411,731-26,413,287 HADHA, GAREM2
    nsv6672785copy number variation1nstd229human GRCh38 chr2: 24,384,939-32,866,867 , GRCh37.p13 chr2: 24,607,808-33,091,934 CENPO, TOGARAM2, 170 more genes
    nsv6669298copy number variation1nstd229human GRCh38 chr2: 26,181,707-26,192,514 , GRCh37.p13 chr2: 26,404,576-26,415,383 HADHA, GAREM2
    nsv6666237copy number variation1nstd229human GRCh38 chr2: 26,215,001-26,384,400 , GRCh37.p13 chr2: 26,437,870-26,607,268 LOC105374334, HADHB, 3 more genes
    nsv6666162copy number variation1nstd229human GRCh38 chr2: 26,222,591-26,222,751 , GRCh37.p13 chr2: 26,445,459-26,445,619 HADHA
    nsv6665209copy number variation1nstd229human GRCh38 chr2: 26,145,357-26,206,699 , GRCh37.p13 chr2: 26,368,226-26,429,568 GAREM2, SMARCE1P6, 2 more genes
    nsv6661369copy number variation1nstd229human GRCh38 chr2: 26,221,301-26,223,100 , GRCh37.p13 chr2: 26,444,169-26,445,968 HADHA
    nsv6659142copy number variation1nstd229human GRCh38 chr2: 25,796,701-26,364,100 , GRCh37.p13 chr2: 26,019,570-26,586,968 KIF3C, ADGRF3, 18 more genes
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 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
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