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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980449copy number variation1nstd102humanrisk factor GRCh37 chr3: 195,693,872-197,376,871 , GRCh38.p12 chr3: 195,967,001-197,650,000 RN7SL434P, RNU6-1279P, 54 more genes
    nsv5975867inversion1nstd209human GRCh38 chr3: 196,245,165-196,619,601 , GRCh37.p13 chr3: 195,972,036-196,346,472 PCYT1A, UBXN7, 17 more genes
    nsv5903304copy number variation1nstd209human GRCh38 chr3: 196,329,047-196,329,974 , GRCh37.p13 chr3: 196,055,918-196,056,845 TM4SF19, TM4SF19-DYNLT2B
    nsv5902688copy number variation1nstd209human GRCh38 chr3: 196,334,789-196,335,210 , GRCh37.p13 chr3: 196,061,660-196,062,081 TM4SF19, TM4SF19-DYNLT2B
    nsv5894889copy number variation1nstd209human GRCh38 chr3: 196,334,807-196,335,088 , GRCh37.p13 chr3: 196,061,678-196,061,959 TM4SF19-DYNLT2B, TM4SF19
    nsv5891362copy number variation1nstd209human GRCh38 chr3: 196,328,950-196,330,064 , GRCh37.p13 chr3: 196,055,821-196,056,935 TM4SF19-DYNLT2B, TM4SF19
    nsv5888778copy number variation1nstd209human GRCh38 chr3: 196,334,822-196,335,521 , GRCh37.p13 chr3: 196,061,693-196,062,392 TM4SF19-DYNLT2B, TM4SF19
    nsv5621065insertion2nstd207human GRCh38 chr3: 196,335,076-196,335,076 , GRCh37.p13 chr3: 196,061,947-196,061,947 TM4SF19-DYNLT2B, TM4SF19
    nsv5613696insertion1nstd207human GRCh38 chr3: 196,335,389-196,335,389 , GRCh37.p13 chr3: 196,062,260-196,062,260 TM4SF19, TM4SF19-DYNLT2B
    nsv5607028insertion1nstd207human GRCh38 chr3: 196,334,825-196,334,825 , GRCh37.p13 chr3: 196,061,696-196,061,696 TM4SF19-DYNLT2B, TM4SF19
    nsv5580297copy number variation1nstd207human GRCh38 chr3: 196,335,076-196,335,145 , GRCh37.p13 chr3: 196,061,947-196,062,016 TM4SF19, TM4SF19-DYNLT2B
    nsv5578985copy number variation1nstd207human GRCh38 chr3: 196,329,047-196,329,974 , GRCh37.p13 chr3: 196,055,918-196,056,845 TM4SF19-DYNLT2B, TM4SF19
    nsv5576844copy number variation1nstd207human GRCh38 chr3: 196,334,893-196,334,961 , GRCh37.p13 chr3: 196,061,764-196,061,832 TM4SF19-DYNLT2B, TM4SF19
    nsv5575676copy number variation1nstd207human GRCh38 chr3: 196,334,808-196,335,018 , GRCh37.p13 chr3: 196,061,679-196,061,889 TM4SF19-DYNLT2B, TM4SF19
    nsv5563557sequence alteration1nstd206human GRCh38 chr3: 196,244,777-196,619,867 , GRCh37.p13 chr3: 195,971,648-196,346,738 PCYT1A, FBXO45, 17 more genes
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5453010copy number variation1nstd206human GRCh38 chr3: 196,320,090-196,322,912 , GRCh37.p13 chr3: 196,046,961-196,049,783 TM4SF19-DYNLT2B, TM4SF19, 1 more genes
    nsv5443435copy number variation1nstd206human GRCh38 chr3: 196,334,885-196,335,623 , GRCh37.p13 chr3: 196,061,756-196,062,494 TM4SF19-DYNLT2B, TM4SF19
    nsv5441885copy number variation1nstd206human GRCh38 chr3: 196,329,087-196,329,968 , GRCh37.p13 chr3: 196,055,958-196,056,839 TM4SF19, TM4SF19-DYNLT2B
    nsv5389374copy number variation1nstd186human GRCh37 chr3: 196,055,947-196,056,845 , GRCh38.p12 chr3: 196,329,076-196,329,974 TM4SF19, TM4SF19-DYNLT2B
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