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Items: 1 to 20 of 199

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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
    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
    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
    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
    nsv6672489copy number variation1nstd229human GRCh38 chr2: 26,170,601-26,184,400 , GRCh37.p13 chr2: 26,393,470-26,407,269 GAREM2
    nsv6669298copy number variation1nstd229human GRCh38 chr2: 26,181,707-26,192,514 , GRCh37.p13 chr2: 26,404,576-26,415,383 HADHA, GAREM2
    nsv6666635copy number variation1nstd229human GRCh38 chr2: 26,173,864-26,174,290 , GRCh37.p13 chr2: 26,396,733-26,397,159 GAREM2
    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
    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
    nsv6628044copy number variation1nstd224human GRCh37 chr2: 26,381,587-26,406,980 , GRCh38.p12 chr2: 26,158,718-26,184,111 GAREM2, PPIL1P1
    nsv6543735inversion1nstd223human GRCh38 chr2: 24,403,241-32,916,237 , GRCh37.p13 chr2: 24,626,110-33,141,304 LOC105374334, LOC107985861, 172 more genes
    nsv6538559inversion1nstd223human GRCh38 chr2: 25,762,333-32,867,002 , GRCh37.p13 chr2: 25,985,202-33,092,069 MIR558, PCARE, 148 more genes
    nsv6344534copy number variation1nstd223human GRCh38 chr2: 24,831,925-32,916,230 , GRCh37.p13 chr2: 25,054,794-33,141,297 LOC102723594, DNAJC5G, 165 more genes
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