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Items: 1 to 20 of 130

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047569inversion1nstd229human GRCh38 chr3: 152,490,812-161,531,961 , GRCh37.p13 chr3: 152,208,601-161,249,749 RPS2P19, LOC112268450, 128 more genes
    nsv6735419copy number variation1nstd229human GRCh38 chr3: 155,200,644-155,415,032 , GRCh37.p13 chr3: 154,918,433-155,132,821 LINC01487, DTWD1P2, 3 more genes
    nsv6732738copy number variation1nstd229human GRCh38 chr3: 155,242,315-155,284,163 , GRCh37.p13 chr3: 154,960,104-155,001,952 LINC01487
    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
    nsv6636805copy number variation1nstd102humanUncertain significance GRCh37 chr3: 154,845,141-155,224,069 , GRCh38.p12 chr3: 155,127,352-155,506,280 DTWD1P2, PLCH1-AS2, 7 more genes
    nsv6561537inversion1nstd223human GRCh38 chr3: 155,242,185-155,242,818 , GRCh37.p13 chr3: 154,959,974-154,960,607 LINC01487
    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
    nsv6311961copy number variation1nstd102humanUncertain significance GRCh37 chr3: 154,801,957-155,551,394 , GRCh38.p12 chr3: 155,084,168-155,833,605 RPL7AP24, STRIT1, 11 more genes
    nsv6290273copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,729,607-157,921,084 , GRCh38.p12 chr3: 143,010,765-158,203,295 LINC02066, TM4SF1-AS1, 206 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
    nsv6112752copy number variation1nstd102humannot provided GRCh37 chr3: 154,548,410-155,021,779 , GRCh38.p12 chr3: 154,830,621-155,303,990 STRIT1, LOC105374170, 3 more genes
    nsv5991687copy number variation1nstd212human GRCh38 chr3: 155,242,125-155,242,209 , GRCh37.p13 chr3: 154,959,914-154,959,998 LINC01487
    nsv5445714copy number variation1nstd206human GRCh38 chr3: 154,528,533-156,057,304 , GRCh37.p13 chr3: 154,246,322-155,775,093 LINC01487, MME, 21 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
    nsv4912509copy number variation1nstd200human GRCh38 chr3: 155,242,315-155,284,161 , GRCh37.p13 chr3: 154,960,104-155,001,950 LINC01487
    nsv4798093copy number variation1nstd200human GRCh37 chr3: 154,960,104-155,001,950 , GRCh38.p12 chr3: 155,242,315-155,284,161 LINC01487
    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
    nsv4680199copy number variation1nstd189human GRCh37.p13 chr3: 154,729,230-155,549,856 , GRCh38.p12 chr3: 155,011,441-155,832,067 MME, SLC33A1, 11 more genes
    nsv4520648copy number variation1nstd166human GRCh37.p13 chr3: 154,525,999-155,025,500 , GRCh38.p12 chr3: 154,808,210-155,307,711 MME, PABPC1P10, 4 more genes
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