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Items: 1 to 20 of 306

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096705copy number variation1nstd102humanUncertain significance GRCh37 chr3: 183,368,145-184,094,097 , GRCh38.p12 chr3: 183,650,357-184,376,309 VWA5B2, MIR1224, 35 more genes
    nsv7096553copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr3: 182,733,226-184,094,097 , GRCh38.p12 chr3: 183,015,438-184,376,309 DVL3, LOC105374247, 51 more genes
    nsv7053971inversion1nstd229human GRCh38 chr3: 183,609,736-184,280,209 , GRCh37.p13 chr3: 183,327,524-183,997,997 HTR3C2P, YEATS2-AS1, 31 more genes
    nsv7044347inversion1nstd229human GRCh38 chr3: 183,875,052-183,883,494 , GRCh37.p13 chr3: 183,592,840-183,601,282 PARL
    nsv6735255copy number variation1nstd229human GRCh38 chr3: 183,863,563-183,863,646 , GRCh37.p13 chr3: 183,581,351-183,581,434 PARL
    nsv6735011copy number variation1nstd229human GRCh38 chr3: 183,868,941-183,873,020 , GRCh37.p13 chr3: 183,586,729-183,590,808 PARL
    nsv6730733copy number variation1nstd229human GRCh38 chr3: 183,877,001-183,878,108 , GRCh37.p13 chr3: 183,594,789-183,595,896 PARL
    nsv6728390copy number variation1nstd229human GRCh38 chr3: 183,883,301-183,929,900 , GRCh37.p13 chr3: 183,601,089-183,647,688 MIR4448, PARL, 3 more genes
    nsv6634384copy number variation1nstd102humanPathogenic GRCh37 chr3: 181,062,175-185,474,509 , GRCh38.p12 chr3: 181,344,387-185,756,721 PRICKLE1P1, KLHL24, 99 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6568575inversion1nstd223human GRCh38 chr3: 183,859,013-183,859,638 , GRCh37.p13 chr3: 183,576,801-183,577,426 PARL
    nsv6567372inversion1nstd223human GRCh38 chr3: 183,874,567-183,877,696 , GRCh37.p13 chr3: 183,592,355-183,595,484 PARL
    nsv6563993inversion1nstd223human GRCh38 chr3: 183,880,868-183,882,057 , GRCh37.p13 chr3: 183,598,656-183,599,845 PARL
    nsv6563009inversion1nstd223human GRCh38 chr3: 183,842,541-183,843,169 , GRCh37.p13 chr3: 183,560,329-183,560,957 PARL
    nsv6556230inversion1nstd223human GRCh38 chr3: 183,875,178-183,876,341 , GRCh37.p13 chr3: 183,592,966-183,594,129 PARL
    nsv6374312copy number variation1nstd223human GRCh38 chr3: 183,881,479-183,891,735 , GRCh37.p13 chr3: 183,599,267-183,609,523 RPSAP31, PARL, 1 more genes
    nsv6358774copy number variation1nstd223human GRCh38 chr3: 183,858,234-183,858,638 , GRCh37.p13 chr3: 183,576,022-183,576,426 PARL
    nsv6357072copy number variation1nstd223human GRCh38 chr3: 183,871,705-183,875,785 , GRCh37.p13 chr3: 183,589,493-183,593,573 PARL
    nsv6315437copy number variation1nstd102humanPathogenic GRCh37 chr3: 183,498,520-197,851,986 , GRCh38.p12 chr3: 183,780,732-198,125,115 LOC105374291, GP5, 315 more genes
    nsv6315366copy number variation1nstd102humanPathogenic GRCh37 chr3: 183,556,940-188,083,060 , GRCh38.p12 chr3: 183,839,152-188,365,272 MASP1, PSMD10P2, 115 more genes
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