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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053767inversion1nstd229human GRCh38 chr3: 158,302,191-159,355,818 , GRCh37.p13 chr3: 158,019,980-159,073,607 RSRC1, GPR79, 17 more genes
    nsv7047586inversion1nstd229human GRCh38 chr3: 158,634,722-159,592,222 , GRCh37.p13 chr3: 158,352,511-159,310,011 LOC100287290, MFSD1, 11 more genes
    nsv7047569inversion1nstd229human GRCh38 chr3: 152,490,812-161,531,961 , GRCh37.p13 chr3: 152,208,601-161,249,749 RPS2P19, LOC112268450, 128 more genes
    nsv6736621copy number variation1nstd229human GRCh38 chr3: 159,273,701-159,828,800 , GRCh37.p13 chr3: 158,991,490-159,546,589 MIR3919, LOC101928351, 6 more genes
    nsv6729787copy number variation1nstd229human GRCh38 chr3: 158,774,329-159,529,256 , GRCh37.p13 chr3: 158,492,118-159,247,045 IQCJ, MIR3919, 7 more genes
    nsv6726205copy number variation1nstd229human GRCh38 chr3: 158,747,475-160,206,668 , GRCh37.p13 chr3: 158,465,264-159,924,455 LOC105374181, MFSD1, 16 more genes
    nsv6723066copy number variation1nstd229human GRCh38 chr3: 159,215,245-159,337,699 , GRCh37.p13 chr3: 158,933,034-159,055,488 SCHIP1, MIR3919, 2 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6365253copy number variation1nstd223human GRCh38 chr3: 158,747,475-160,206,664 , GRCh37.p13 chr3: 158,465,264-159,924,451 IL12A-AS1, RPL35AP9, 16 more genes
    nsv6364493copy number variation1nstd223human GRCh38 chr3: 159,278,601-159,285,800 , GRCh37.p13 chr3: 158,996,390-159,003,589 IQCJ-SCHIP1, SCHIP1, 1 more genes
    nsv6313678copy number variation1nstd102humanPathogenic GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046 RNU6-901P, RPL32P8, 229 more genes
    nsv6313664copy number variation1nstd102humanUncertain significance GRCh37 chr3: 156,768,935-160,158,553 , GRCh38.p12 chr3: 157,051,146-160,440,765 LOC105374179, RPL15P6, 49 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 LOC102724145, C3orf80, 273 more genes
    nsv6134788copy number variation1nstd213human GRCh37 chr3: 155,010,000-169,630,001 , GRCh38.p12 chr3: 155,292,211-169,912,213 , BCHE, 171 more genes
    nsv5439255copy number variation1nstd206human GRCh38 chr3: 159,282,580-159,282,684 , GRCh37.p13 chr3: 159,000,369-159,000,473 IQCJ-SCHIP1, SCHIP1, 1 more genes
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4684209copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822 MTAPP1, PLS1, 339 more genes
    nsv4684148copy number variation1nstd102humanUncertain significance GRCh37 chr3: 156,812,581-160,154,747 , GRCh38.p12 chr3: 157,094,792-160,436,959 RSRC1, SMC4, 48 more genes
    nsv4680693copy number variation1nstd189human GRCh37.p13 chr3: 158,341,623-159,202,634 , GRCh38.p12 chr3: 158,623,834-159,484,845 , RARRES1, 12 more genes
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