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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6817627copy number variation1nstd229human GRCh38 chr6: 131,459,401-131,471,400 , GRCh37.p13 chr6: 131,780,541-131,792,540 RPL21P67
    nsv6808954copy number variation1nstd229human GRCh38 chr6: 131,464,715-132,189,626 , GRCh37.p13 chr6: 131,785,855-132,510,766 LOC100421775, MIR548H5, 14 more genes
    nsv6808420copy number variation1nstd229human GRCh38 chr6: 130,549,501-131,568,700 , GRCh37.p13 chr6: 130,870,646-131,889,840 LOC105378002, LOC105378005, 8 more genes
    nsv6802352copy number variation1nstd229human GRCh38 chr6: 131,461,451-131,471,096 , GRCh37.p13 chr6: 131,782,591-131,792,236 RPL21P67
    nsv6799098copy number variation1nstd229human GRCh38 chr6: 131,462,512-131,467,985 , GRCh37.p13 chr6: 131,783,652-131,789,125 RPL21P67
    nsv6798159copy number variation1nstd229human GRCh38 chr6: 131,401,393-131,490,911 , GRCh37.p13 chr6: 131,722,533-131,812,051 LOC105378005, RPL21P67
    nsv6631167copy number variation1nstd224human GRCh37 chr6: 131,728,258-131,809,920 , GRCh38.p12 chr6: 131,407,118-131,488,780 LOC105378005, RPL21P67
    nsv6600355copy number variation1nstd223human GRCh38 chr6: 131,462,512-131,467,981 , GRCh37.p13 chr6: 131,783,652-131,789,121 RPL21P67
    nsv6564345inversion1nstd223human GRCh38 chr6: 131,467,931-131,468,362 , GRCh37.p13 chr6: 131,789,071-131,789,502 RPL21P67
    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
    nsv6313685copy number variation1nstd102humanUncertain significance GRCh37 chr6: 130,949,600-131,924,268 , GRCh38.p12 chr6: 130,628,455-131,603,128 ARG1, LOC100421246, 10 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
    nsv5968494inversion1nstd209human GRCh38 chr6: 125,606,968-134,343,905 , GRCh37.p13 chr6: 125,928,114-134,665,043 , ARG1, 137 more genes
    nsv5906945copy number variation1nstd209human GRCh38 chr6: 123,301,756-132,349,395 , GRCh37.p13 chr6: 123,622,901-132,670,534 , LOC105377999, 105 more genes
    nsv5554649sequence alteration1nstd206human GRCh38 chr6: 131,260,840-131,506,065 , GRCh37.p13 chr6: 131,581,980-131,827,205 , AKAP7, 2 more genes
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