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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148221copy number variation1nstd102humanPathogenic GRCh38 chr6: 150,905,553-158,511,926 , GRCh37.p13 chr6: 151,226,689-158,932,958 RNU6-824P, LOC105378067, 97 more genes
    nsv7139147copy number variation1nstd232human GRCh37.p13 chr6: 151,771,542-151,771,620 , GRCh38.p12 chr6: 151,450,407-151,450,485 RMND1, ARMT1
    nsv7042877inversion1nstd229human GRCh38 chr6: 149,723,719-152,206,487 , GRCh37.p13 chr6: 150,044,855-152,527,622 MTHFD1L, RAET1F, 48 more genes
    nsv7041422inversion1nstd229human GRCh38 chr6: 150,201,394-154,373,035 , GRCh37.p13 chr6: 150,522,530-154,694,169 MTHFD1L, MYCT1, 56 more genes
    nsv6817297copy number variation1nstd229human GRCh38 chr6: 151,370,892-151,716,763 , GRCh37.p13 chr6: 151,692,027-152,037,898 ARMT1, HSPA8P15, 6 more genes
    nsv6816139copy number variation1nstd229human GRCh38 chr6: 151,077,301-151,497,900 , GRCh37.p13 chr6: 151,398,437-151,819,035 LOC102723831, ARMT1, 13 more genes
    nsv6807402copy number variation1nstd229human GRCh38 chr6: 151,075,901-151,743,600 , GRCh37.p13 chr6: 151,397,037-152,064,735 RNU6-813P, ARMT1, 16 more genes
    nsv6802272copy number variation1nstd229human GRCh38 chr6: 151,377,122-151,459,806 , GRCh37.p13 chr6: 151,698,257-151,780,941 ZBTB2, RMND1, 2 more genes
    nsv6631091copy number variation1nstd224human GRCh37 chr6: 151,686,905-151,859,314 , GRCh38.p12 chr6: 151,365,770-151,538,179 RMND1, ZBTB2, 3 more genes
    nsv6630679copy number variation1nstd224human GRCh37 chr6: 151,734,061-151,854,111 , GRCh38.p12 chr6: 151,412,926-151,532,976 ARMT1, RMND1, 2 more genes
    nsv6630678copy number variation1nstd224human GRCh37 chr6: 150,525,260-152,157,881 , GRCh38.p12 chr6: 150,204,124-151,836,746 MTHFD1L, ARMT1, 27 more genes
    nsv6617098copy number variation1nstd223human GRCh38 chr6: 151,469,376-151,481,946 , GRCh37.p13 chr6: 151,790,511-151,803,081 ARMT1
    nsv6609650copy number variation1nstd223human GRCh38 chr6: 151,450,170-151,451,179 , GRCh37.p13 chr6: 151,771,305-151,772,314 ARMT1, RMND1
    nsv6605346copy number variation1nstd223human GRCh38 chr6: 151,448,501-151,456,000 , GRCh37.p13 chr6: 151,769,636-151,777,135 ARMT1, RMND1
    nsv6567552inversion1nstd223human GRCh38 chr6: 151,459,127-151,460,105 , GRCh37.p13 chr6: 151,780,262-151,781,240 ARMT1
    nsv6565509inversion1nstd223human GRCh38 chr6: 151,459,805-151,459,987 , GRCh37.p13 chr6: 151,780,940-151,781,122 ARMT1
    nsv6564527inversion1nstd223human GRCh38 chr6: 150,782,887-160,100,808 , GRCh37.p13 chr6: 151,104,023-160,521,840 RPL31P29, RPL17P24, 139 more genes
    nsv6562231inversion1nstd223human GRCh38 chr6: 150,783,018-160,100,808 , GRCh37.p13 chr6: 151,104,154-160,521,840 ARMT1, LOC102723831, 139 more genes
    nsv6180268copy number variation1nstd214human GRCh38 chr6: 151,450,407-151,450,485 , GRCh37.p13 chr6: 151,771,542-151,771,620 RMND1, ARMT1
    nsv6007192copy number variation1nstd212human GRCh38 chr6: 151,450,493-151,450,592 , GRCh37.p13 chr6: 151,771,628-151,771,727 ARMT1, RMND1
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