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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054595inversion1nstd229human GRCh38 chr2: 129,115,794-130,999,381 , GRCh37.p13 chr2: 129,873,367-131,756,954 LOC646674, CYP4F27P, 65 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
    nsv7053338inversion1nstd229human GRCh38 chr2: 129,419,773-131,102,874 , GRCh37.p13 chr2: 130,177,346-131,860,447 RPL19P4, PRSS40A, 65 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
    nsv7048610inversion1nstd229human GRCh38 chr2: 129,502,833-131,219,594 , GRCh37.p13 chr2: 130,260,406-131,977,167 LOC105373614, TRE-TTC1-1, 67 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
    nsv7040855inversion1nstd229human GRCh38 chr2: 130,061,198-131,276,586 , GRCh37.p13 chr2: 130,818,771-132,034,159 NF1P8, MTND4P27, 53 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
    nsv7039384inversion1nstd229human GRCh38 chr2: 130,267,565-131,389,372 , GRCh37.p13 chr2: 131,025,138-132,146,945 TEKT4P3, CFC1, 65 more genes
    nsv6695072copy number variation1nstd229human GRCh38 chr2: 130,750,752-131,009,581 , GRCh37.p13 chr2: 131,508,325-131,767,154 CYCSP8, AMER3, 1 more genes
    nsv6692793copy number variation1nstd229human GRCh38 chr2: 130,754,914-130,754,970 , GRCh37.p13 chr2: 131,512,487-131,512,543 AMER3
    nsv6688860copy number variation1nstd229human GRCh38 chr2: 130,722,251-130,845,344 , GRCh37.p13 chr2: 131,479,824-131,602,917 GPR148, CYCSP8, 2 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
    nsv6636768copy number variation1nstd102humanUncertain significance GRCh37 chr2: 131,452,093-132,035,609 , GRCh38.p12 chr2: 130,694,520-131,278,036 ARHGEF4, LOC440910, 11 more genes
    nsv6627516copy number variation1nstd224human GRCh37 chr2: 131,482,506-131,933,628 , GRCh38.p12 chr2: 130,724,933-131,176,055 ARHGEF4, PLEKHB2, 5 more genes
    nsv6627326copy number variation1nstd224human GRCh37 chr2: 131,484,635-131,951,961 , GRCh38.p12 chr2: 130,727,062-131,194,388 ARHGEF4, PLEKHB2, 6 more genes
    nsv6555058inversion1nstd223human GRCh38 chr2: 130,185,479-131,489,305 , GRCh37.p13 chr2: 130,943,052-132,246,878 SSBP3P2, LINC01120, 78 more genes
    nsv6553476inversion1nstd223human GRCh38 chr2: 130,061,029-131,276,582 , GRCh37.p13 chr2: 130,818,602-132,034,155 MTND4P27, MTND6P8, 53 more genes
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