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Items: 1 to 20 of 101

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3896739copy number variation1nstd102humanBenign GRCh37 chr9: 19,273,374-19,346,941 , GRCh38.p12 chr9: 19,273,376-19,346,943 DENND4C
    nsv3907309copy number variation1nstd102humanBenign GRCh37 chr9: 19,358,608-19,367,467 , GRCh38.p12 chr9: 19,358,610-19,367,469 DENND4C
    nsv3899076copy number variation1nstd102humanBenign GRCh37 chr9: 19,358,608-19,364,042 , GRCh38.p12 chr9: 19,358,610-19,364,044 DENND4C
    nsv3902556copy number variation1nstd102humanBenign GRCh37 chr9: 19,358,608-19,359,580 , GRCh38.p12 chr9: 19,358,610-19,359,582 DENND4C
    nsv3893925copy number variation1nstd102humanBenign GRCh37 chr9: 19,273,374-19,274,060 , GRCh38.p12 chr9: 19,273,376-19,274,062 DENND4C
    nsv3894211copy number variation1nstd102humanBenign GRCh37 chr9: 19,273,582-19,274,154 , GRCh38.p12 chr9: 19,273,584-19,274,156 DENND4C
    nsv3898932copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,236,488-19,322,101 , GRCh38.p12 chr9: 19,236,490-19,322,103 DENND4C
    nsv4729438copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,313,795-19,367,790 , GRCh38.p12 chr9: 19,313,797-19,367,792 DENND4C
    nsv3972402copy number variation1nstd102humanLikely benign GRCh37 chr9: 19,228,097-19,441,405 , GRCh38.p12 chr9: 19,228,099-19,441,407 DENND4C, NDUFA5P3, 2 more genes
    nsv4729262copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,108,473-19,329,836 , GRCh38.p12 chr9: 19,108,475-19,329,838 DENND4C, RPS6P10, 1 more genes
    nsv6315395copy number variation1nstd102humanPathogenic GRCh37 chr9: 4,992,582-19,322,101 , GRCh38.p12 chr9: 4,992,582-19,322,103 DENND4C, FREM1, 142 more genes
    nsv3912247copy number variation1nstd102humanPathogenic NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981 DENND4C, ALOX15P2, 2184 more genes
    nsv3890420copy number variation1nstd102humanPathogenic GRCh37 chr9: 10,590-141,122,247 , GRCh38.p12 chr9: 10,590-138,231,797 DENND4C, TBC1D13, 2183 more genes
    nsv3905118copy number variation1nstd102humanPathogenic GRCh37 chr9: 10,590-141,114,095 , GRCh38.p12 chr9: 10,590-138,223,645 DENND4C, MIR219A2, 2183 more genes
    nsv3891842copy number variation1nstd102humanPathogenic GRCh37 chr9: 10,590-141,107,672 , GRCh38.p12 chr9: 10,590-138,217,222 DENND4C, OR13C1P, 2183 more genes
    nsv3895453copy number variation1nstd102humanPathogenic GRCh37 chr9: 46,587-141,066,491 , GRCh38.p12 chr9: 46,587-138,172,039 DENND4C, RPL19P15, 2176 more genes
    nsv3900967copy number variation1nstd102humanPathogenic GRCh37 chr9: 163,131-141,122,114 , GRCh38.p12 chr9: 163,131-138,231,664 DENND4C, BANCR, 2173 more genes
    nsv3907479copy number variation1nstd102humanPathogenic GRCh37 chr9: 62,525-141,006,407 , GRCh38.p12 chr9: 62,525-138,111,955 DENND4C, OR2AM1P, 2174 more genes
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 DENND4C, TDRD7, 2170 more genes
    nsv3919257copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-141,073,897 , GRCh38 chr9: 204,193-138,179,445 , NCBI36 chr9: 194,193-140,193,718 DENND4C, LOC107987031, 2169 more genes
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