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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3905232copy number variation1nstd102humanPathogenic GRCh38 chr3: 32,241-12,681,483 , GRCh37 chr3: 73,914-12,722,982 , NCBI36 chr3: 48,914-12,697,982 TADA3, OR7E122P, 163 more genes
    nsv3885461copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-12,575,409 , GRCh38.p12 chr3: 20,213-12,533,910 TADA3, MARK2P14, 160 more genes
    nsv6636276copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,892-11,679,509 , GRCh38.p12 chr3: 20,214-11,638,035 TADA3, RPL23AP39, 144 more genes
    nsv3906827copy number variation1nstd102humanPathogenic GRCh38 chr3: 32,241-11,379,835 , GRCh37 chr3: 73,914-11,421,309 , NCBI36 chr3: 48,914-11,396,309 TADA3, LOC107986040, 142 more genes
    nsv3895550copy number variation1nstd102humanPathogenic GRCh38 chr3: 20,213-11,221,602 , NCBI36 chr3: 36,891-11,238,288 , GRCh37 chr3: 61,891-11,263,288 TADA3, SRGAP3, 141 more genes
    nsv3900952copy number variation1nstd102humanPathogenic GRCh38 chr3: 52,266-11,089,569 , NCBI36 chr3: 68,949-11,106,255 , GRCh37 chr3: 93,949-11,131,255 TADA3, RPUSD3, 137 more genes
    nsv3900980copy number variation1nstd102humanPathogenic GRCh37 chr3: 73,914-10,672,995 , GRCh38 chr3: 32,241-10,631,310 , NCBI36 chr3: 48,914-10,647,995 TADA3, MIR885, 131 more genes
    nsv3892568copy number variation1nstd102humanPathogenic NCBI36 chr3: 705,581-11,067,828 , GRCh37 chr3: 730,581-11,092,828 , GRCh38 chr3: 688,897-11,051,142 TADA3, DUSP5P2, 126 more genes
    nsv3894686copy number variation1nstd102humanPathogenic NCBI36 chr3: 48,914-10,339,808 , GRCh38 chr3: 32,241-10,323,124 , GRCh37 chr3: 73,914-10,364,808 TADA3, RPL21P17, 128 more genes
    nsv4674715copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-10,287,825 , GRCh38.p12 chr3: 20,213-10,246,141 TADA3, LOC105376944, 122 more genes
    nsv3889023copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-10,104,842 , GRCh38.p12 chr3: 20,213-10,063,158 TADA3, TTLL3, 118 more genes
    nsv6636296copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,892-9,899,605 , GRCh38.p12 chr3: 20,214-9,857,921 TADA3, GRM7-AS1, 101 more genes
    nsv7148084copy number variation1nstd102humanPathogenic GRCh37 chr3: 3,669,542-9,937,745 , GRCh38.p12 chr3: 3,627,858-9,896,061 TADA3, LOC105376943, 71 more genes
    nsv3880780copy number variation1nstd102humanPathogenic GRCh37 chr3: 8,922,160-12,338,637 , GRCh38.p12 chr3: 8,880,476-12,297,138 TADA3, IL17RC, 77 more genes
    nsv3882563copy number variation1nstd102humanPathogenic GRCh37 chr3: 6,842,555-10,153,209 , GRCh38.p12 chr3: 6,800,868-10,111,525 TADA3, LOC107984112, 57 more genes
    nsv3911723copy number variation1nstd102humanPathogenic GRCh37 chr3: 9,436,558-11,732,086 , GRCh38 chr3: 9,394,874-11,690,612 , NCBI36 chr3: 9,411,558-11,707,086 TADA3, FANCD2, 57 more genes
    nsv3924927copy number variation1nstd102humanPathogenic GRCh37 chr3: 9,695,981-10,270,371 , NCBI36 chr3: 9,670,981-10,245,371 , GRCh38 chr3: 9,654,297-10,228,687 TADA3, CIDECP1, 30 more genes
    nsv3910678copy number variation1nstd102humanPathogenic NCBI36 chr3: 9,410,033-9,972,855 , GRCh37 chr3: 9,435,033-9,997,855 , GRCh38 chr3: 9,393,349-9,956,171 TADA3, LHFPL4, 22 more genes
    nsv3884616copy number variation1nstd102humanPathogenic GRCh37 chr3: 9,666,380-10,028,247 , GRCh38.p12 chr3: 9,624,696-9,986,563 TADA3, CIDEC, 19 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 TADA3, RNU4-62P, 2880 more genes
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