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Items: 1 to 20 of 243

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098929copy number variation1nstd102humanPathogenic GRCh38 chr3: 195,950,438-197,629,463 , GRCh37.p13 chr3: 195,677,309-197,356,334 LINC01063, RNF168, 52 more genes
    nsv7098781copy number variation1nstd102humanUncertain significance GRCh37 chr3: 195,591,052-197,682,644 , GRCh38.p12 chr3: 195,864,181-197,955,773 ZDHHC19, DLG1, 68 more genes
    nsv7055557inversion1nstd229human GRCh38 chr3: 195,655,301-197,630,693 , GRCh37.p13 chr3: 195,382,172-197,357,564 MIR570HG, RN7SL434P, 66 more genes
    nsv7053852inversion1nstd229human GRCh38 chr3: 195,653,753-197,300,599 , GRCh37.p13 chr3: 195,380,624-197,027,470 NCBP2-AS1, SMCO1, 59 more genes
    nsv7053446inversion1nstd229human GRCh38 chr3: 195,340,377-197,478,980 , GRCh37.p13 chr3: 195,061,106-197,205,851 CEP19, ACAP2, 73 more genes
    nsv7050481inversion1nstd229human GRCh38 chr3: 196,292,084-196,493,779 , GRCh37.p13 chr3: 196,018,955-196,220,650 RNF168, TM4SF19-AS1, 10 more genes
    nsv7044295inversion1nstd229human GRCh38 chr3: 195,547,271-197,153,236 , GRCh37.p13 chr3: 195,274,089-196,880,107 SDHAP1, NCBP2AS2, 64 more genes
    nsv7044261inversion1nstd229human GRCh38 chr3: 195,438,610-197,225,061 , GRCh37.p13 chr3: 195,159,339-196,951,932 MUC4, RPL24P6, 67 more genes
    nsv6728901copy number variation1nstd229human GRCh38 chr3: 196,423,436-196,432,179 , GRCh37.p13 chr3: 196,150,307-196,159,050 UBXN7, UBXN7-AS1
    nsv6728821copy number variation1nstd229human GRCh38 chr3: 196,202,777-196,997,902 , GRCh37.p13 chr3: 195,929,648-196,724,773 DYNLT2B, RN7SL434P, 35 more genes
    nsv6725478copy number variation1nstd229human GRCh38 chr3: 196,207,115-197,269,106 , GRCh37.p13 chr3: 195,933,986-196,995,977 PAK2, LINC01063, 38 more genes
    nsv6725286copy number variation1nstd229human GRCh38 chr3: 196,377,963-196,914,388 , GRCh37.p13 chr3: 196,104,834-196,641,259 RNF168, RNU6-646P, 19 more genes
    nsv6636887copy number variation1nstd102humanPathogenic GRCh37 chr3: 195,690,228-197,356,334 , GRCh38.p12 chr3: 195,963,357-197,629,463 LOC105374307, NRROS, 52 more genes
    nsv6636275copy number variation1nstd102humanUncertain significance GRCh37 chr3: 195,790,857-196,543,483 , GRCh38.p12 chr3: 196,063,986-196,816,612 RN7SL738P, RN7SL434P, 31 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
    nsv6315456copy number variation1nstd102humanPathogenic GRCh37 chr3: 195,703,615-197,386,180 , GRCh38.p12 chr3: 195,976,744-197,659,309 PIGX, MELTF-AS1, 54 more genes
    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
    nsv6314812copy number variation1nstd102humanPathogenic GRCh38 chr3: 195,832,526-197,342,279 , GRCh37.p13 chr3: 195,559,397-197,069,150 LOC100133326, MIR4797, 54 more genes
    nsv6291411copy number variation1nstd102humanUncertain significance GRCh37 chr3: 195,993,691-197,851,986 , GRCh38.p12 chr3: 196,266,820-198,125,115 IQCG, PAK2, 62 more genes
    nsv6291306copy number variation1nstd102humanPathogenic GRCh37 chr3: 195,914,129-196,804,639 , GRCh38.p12 chr3: 196,187,258-197,077,768 RPS29P3, PAK2, 38 more genes
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