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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055259inversion1nstd229human GRCh38 chr2: 131,382,010-131,405,781 , GRCh37.p13 chr2: 132,139,583-132,163,354 MTND2P18, MTATP6P4, 8 more genes
    nsv7054369inversion1nstd229human GRCh38 chr2: 130,169,998-131,503,917 , GRCh37.p13 chr2: 130,927,571-132,261,490 CYP4F31P, RNU6-127P, 80 more genes
    nsv7054036inversion1nstd229human GRCh38 chr2: 130,188,517-131,488,300 , GRCh37.p13 chr2: 130,946,090-132,245,873 PLEKHB2, GPR148, 77 more genes
    nsv7049181inversion1nstd229human GRCh38 chr2: 130,136,548-131,548,052 , GRCh37.p13 chr2: 130,894,121-132,305,625 NMTRQ-TTG7-1, LOC105373618, 84 more genes
    nsv7043991inversion1nstd229human GRCh38 chr2: 130,170,282-131,542,431 , GRCh37.p13 chr2: 130,927,855-132,300,004 MTND2P22, MTND5P29, 82 more genes
    nsv7042920inversion1nstd229human GRCh38 chr2: 130,241,080-131,493,852 , GRCh37.p13 chr2: 130,998,653-132,251,425 NMTRS-TGA2-1, RNU6-127P, 75 more genes
    nsv7039843inversion1nstd229human GRCh38 chr2: 130,135,157-131,537,855 , GRCh37.p13 chr2: 130,892,730-132,295,428 CYP4F30P, RNU6-473P, 84 more genes
    nsv6695715copy number variation1nstd229human GRCh38 chr2: 131,189,090-132,220,664 , GRCh37.p13 chr2: 131,946,663-132,978,237 LOC647996, MTND5P23, 52 more genes
    nsv6694899copy number variation1nstd229human GRCh38 chr2: 131,386,409-131,418,991 , GRCh37.p13 chr2: 132,143,982-132,176,564 MED15P3, MTND1P26, 2 more genes
    nsv6691161copy number variation1nstd229human GRCh38 chr2: 131,381,601-131,531,500 , GRCh37.p13 chr2: 132,139,174-132,289,073 MZT2A, MTATP6P4, 16 more genes
    nsv6679692copy number variation1nstd229human GRCh38 chr2: 128,625,642-138,426,614 , GRCh37.p13 chr2: 129,383,216-139,184,184 MTND4P27, LOC646674, 194 more genes
    nsv6636398copy number variation1nstd102humanUncertain significance GRCh37 chr2: 132,058,665-133,163,759 , GRCh38.p12 chr2: 131,301,092-132,406,186 LOC105373622, MTND4LP28, 55 more genes
    nsv6636359copy number variation1nstd102humanUncertain significance GRCh37 chr2: 131,974,176-132,269,102 , GRCh38.p12 chr2: 131,216,603-131,511,529 SMPD4BP, LOC100420006, 32 more genes
    nsv6636193copy number variation1nstd102humanUncertain significance GRCh37 chr2: 131,974,176-132,280,823 , GRCh38.p12 chr2: 131,216,603-131,523,250 MTND3P18, LOC100420006, 33 more genes
    nsv6634402copy number variation1nstd102humanUncertain significance GRCh37 chr2: 131,853,044-133,195,255 , GRCh38.p12 chr2: 131,095,471-132,437,682 MTND2P18, LOC100420006, 66 more genes
    nsv6627693copy number variation1nstd224human GRCh37 chr2: 132,077,379-132,298,468 , GRCh38.p12 chr2: 131,319,806-131,540,895 RHOQP2, MED15P4, 28 more genes
    nsv6627692copy number variation1nstd224human GRCh37 chr2: 132,077,379-132,241,650 , GRCh38.p12 chr2: 131,319,806-131,484,077 MTATP6P4, MTCO1P18, 24 more genes
    nsv6627691copy number variation1nstd224human GRCh37 chr2: 132,057,166-132,290,948 , GRCh38.p12 chr2: 131,299,593-131,533,375 FAR2P4, MTATP6P4, 31 more genes
    nsv6627687copy number variation1nstd224human GRCh37 chr2: 131,951,961-132,298,468 , GRCh38.p12 chr2: 131,194,388-131,540,895 GNAQP1, SMPD4BP, 36 more genes
    nsv6627330copy number variation1nstd224human GRCh37 chr2: 132,077,379-132,339,510 , GRCh38.p12 chr2: 131,319,806-131,581,937 LINC01120, NOC2LP2, 28 more genes
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