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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054664inversion1nstd229human GRCh38 chr6: 132,694,770-132,697,718 , GRCh37.p13 chr6: 133,015,909-133,018,857 CCNG1P1, VNN1
    nsv7054647inversion1nstd229human GRCh38 chr6: 125,609,155-134,343,808 , GRCh37.p13 chr6: 125,930,301-134,664,946 RPS12, TMEM244, 130 more genes
    nsv7053719inversion1nstd229human GRCh38 chr6: 125,606,974-134,343,957 , GRCh37.p13 chr6: 125,928,120-134,665,095 SNORD100, SLC18B1, 130 more genes
    nsv7040961inversion1nstd229human GRCh38 chr6: 131,090,546-134,695,837 , GRCh37.p13 chr6: 131,411,686-135,016,975 ENPP3, MOXD1, 70 more genes
    nsv7038109inversion1nstd229human GRCh38 chr6: 125,606,921-134,343,957 , GRCh37.p13 chr6: 125,928,067-134,665,095 PTPRK-AS1, MED23, 130 more genes
    nsv6814039copy number variation1nstd229human GRCh38 chr6: 132,566,240-132,763,774 , GRCh37.p13 chr6: 132,887,379-133,084,913 TAAR2, TAAR5, 10 more genes
    nsv6812137copy number variation1nstd229human GRCh38 chr6: 132,663,798-132,745,890 , GRCh37.p13 chr6: 132,984,937-133,067,029 CCNG1P1, VNN3P, 3 more genes
    nsv6809094copy number variation1nstd229human GRCh38 chr6: 132,661,447-132,706,146 , GRCh37.p13 chr6: 132,982,586-133,027,285 CCNG1P1, HLFP1, 1 more genes
    nsv6805353copy number variation1nstd229human GRCh38 chr6: 132,604,434-132,995,678 , GRCh37.p13 chr6: 132,925,573-133,316,817 TAAR3P, SNORD101, 16 more genes
    nsv6800971copy number variation1nstd229human GRCh38 chr6: 132,710,505-132,715,973 , GRCh37.p13 chr6: 133,031,644-133,037,112 VNN1
    nsv6631168copy number variation1nstd224human GRCh37 chr6: 133,032,668-133,454,738 , GRCh38.p12 chr6: 132,711,529-133,133,599 RPS12, VNN1, 12 more genes
    nsv6617051copy number variation1nstd223human GRCh38 chr6: 132,613,927-132,764,581 , GRCh37.p13 chr6: 132,935,066-133,085,720 VNN1, CCNG1P1, 6 more genes
    nsv6606163copy number variation1nstd223human GRCh38 chr6: 132,604,434-132,995,678 , GRCh37.p13 chr6: 132,925,573-133,316,817 HLFP1, VNN2, 16 more genes
    nsv6573671inversion1nstd223human GRCh38 chr6: 132,709,496-132,710,089 , GRCh37.p13 chr6: 133,030,635-133,031,228 VNN1
    nsv6563707inversion1nstd223human GRCh38 chr6: 125,606,968-134,343,906 , GRCh37.p13 chr6: 125,928,114-134,665,044 TAAR2, LOC105377996, 130 more genes
    nsv6315321copy number variation1nstd102humanPathogenic GRCh38 chr6: 115,941,808-133,892,653 , GRCh37.p13 chr6: 116,262,971-134,213,791 SLC18B1, ARHGAP18, 223 more genes
    nsv6290946copy number variation1nstd102humanPathogenic GRCh37 chr6: 130,769,034-136,009,217 , GRCh38.p12 chr6: 130,447,889-135,688,079 LOC105378004, LINC01010, 89 more genes
    nsv6290724copy number variation1nstd102humanUncertain significance GRCh37 chr6: 132,875,123-133,509,642 , GRCh38.p12 chr6: 132,553,984-133,188,503 RPS12, HMGB1P13, 23 more genes
    nsv6077386insertion1nstd212human GRCh38 chr6: 132,706,868-132,706,868 , GRCh37.p13 chr6: 133,028,007-133,028,007 VNN1
    nsv6016760copy number variation1nstd212human GRCh38 chr6: 132,692,640-132,692,703 , GRCh37.p13 chr6: 133,013,779-133,013,842 VNN1
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