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Items: 1 to 20 of 264

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964124insertion1nstd209human GRCh38 chr6: 166,923,228-166,923,228 , GRCh37.p13 chr6: 167,336,716-167,336,716 RNASET2
    nsv5925202copy number variation1nstd209human GRCh38 chr6: 166,930,725-166,930,906 , GRCh37.p13 chr6: 167,344,213-167,344,394 RNASET2
    nsv5922688copy number variation1nstd209human GRCh38 chr6: 166,925,011-166,925,171 , GRCh37.p13 chr6: 167,338,499-167,338,659 RNASET2
    nsv5921425copy number variation1nstd209human GRCh38 chr6: 166,925,387-166,925,470 , GRCh37.p13 chr6: 167,338,875-167,338,958 RNASET2
    nsv5919426copy number variation1nstd209human GRCh38 chr6: 166,955,255-166,955,334 , GRCh37.p13 chr6: 167,368,743-167,368,822 RNASET2
    nsv5915204copy number variation1nstd209human GRCh38 chr6: 166,930,794-166,930,871 , GRCh37.p13 chr6: 167,344,282-167,344,359 RNASET2
    nsv5909646copy number variation1nstd209human GRCh38 chr6: 166,954,752-166,978,700 , GRCh37.p13 chr6: 167,368,240-167,392,188 RNASET2, LOC105378120
    nsv5844196copy number variation1nstd209human GRCh38 chr6: 166,954,710-166,961,355 , GRCh37.p13 chr6: 167,368,198-167,374,843 RNASET2
    nsv5673597copy number variation1nstd102humanPathogenic GRCh37 chr6: 167,356,507-167,369,670 , GRCh38.p12 chr6: 166,943,019-166,956,182 LOC105378119, RNASET2
    nsv5578460copy number variation1nstd207human GRCh38 chr6: 166,925,387-166,925,470 , GRCh37.p13 chr6: 167,338,875-167,338,958 RNASET2
    nsv5577581copy number variation1nstd207human GRCh38 chr6: 166,955,290-166,955,356 , GRCh37.p13 chr6: 167,368,778-167,368,844 RNASET2
    nsv5536908insertion1nstd206human GRCh38 chr6: 166,930,620-166,930,642 , GRCh37.p13 chr6: 167,344,108-167,344,130 RNASET2
    nsv5470221copy number variation1nstd206human GRCh38 chr6: 166,952,885-166,972,100 , GRCh37.p13 chr6: 167,366,373-167,385,588 LOC105378120, RNASET2
    nsv5363548translocation1nstd200human GRCh38 chr8: 97,775,791-97,775,791 , GRCh38 chr6: 166,920,475-166,920,475 , GRCh37.p13 chr6: 167,333,963-167,333,963 , GRCh37.p13 chr8: 98,788,019-98,788,019 LAPTM4B, RNASET2
    nsv4750047copy number variation1nstd199human GRCh37 chr6: 167,368,661-167,368,782 , GRCh38.p12 chr6: 166,955,173-166,955,294 RNASET2
    nsv4732238copy number variation1nstd199human GRCh37 chr6: 167,338,877-167,338,961 , GRCh38.p12 chr6: 166,925,389-166,925,473 RNASET2
    nsv4729645copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 166,083,476-170,919,482 , GRCh38.p12 chr6: 165,669,988-170,610,394 CCR6, GNG5P1, 118 more genes
    nsv4675923copy number variation1nstd102humanPathogenic GRCh37 chr6: 162,452,035-170,919,482 , GRCh38.p12 chr6: 162,031,003-170,610,394 TRE-TTC15-1, LOC105378137, 148 more genes
    nsv4675281copy number variation1nstd102humanPathogenic GRCh37 chr6: 162,661,108-170,919,482 , GRCh38.p12 chr6: 162,240,076-170,610,394 LOC105378127, LOC105378130, 148 more genes
    nsv4608607copy number variation1nstd183human GRCh37 chr6: 167,185,964-167,367,044 , GRCh38.p12 chr6: 166,772,476-166,953,556 RPS6KA2, RNASET2, 2 more genes
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