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Items: 1 to 20 of 259

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138938copy number variation1nstd232human GRCh37.p13 chr6: 134,353,543-134,353,608 , GRCh38.p12 chr6: 134,032,405-134,032,470 SLC2A12
    nsv7056745inversion1nstd229human GRCh38 chr6: 134,008,379-134,013,048 , GRCh37.p13 chr6: 134,329,517-134,334,186 SLC2A12, LOC100421250
    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
    nsv6814876copy number variation1nstd229human GRCh38 chr6: 134,023,661-134,023,717 , GRCh37.p13 chr6: 134,344,799-134,344,855 SLC2A12
    nsv6811160copy number variation1nstd229human GRCh38 chr6: 133,985,966-134,381,629 , GRCh37.p13 chr6: 134,307,104-134,702,767 RN7SL408P, HMGA1P7, 8 more genes
    nsv6636667copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,522,860-134,541,311 , GRCh38.p12 chr6: 133,201,721-134,220,173 LINC01312, SGK1, 11 more genes
    nsv6613002copy number variation1nstd223human GRCh38 chr6: 134,030,856-134,033,105 , GRCh37.p13 chr6: 134,351,994-134,354,243 SLC2A12
    nsv6609533copy number variation1nstd223human GRCh38 chr6: 134,037,180-134,040,052 , GRCh37.p13 chr6: 134,358,318-134,361,190 SLC2A12
    nsv6605787copy number variation1nstd223human GRCh38 chr6: 133,993,002-133,993,400 , GRCh37.p13 chr6: 134,314,140-134,314,538 SLC2A12
    nsv6601871copy number variation1nstd223human GRCh38 chr6: 133,991,949-133,992,672 , GRCh37.p13 chr6: 134,313,087-134,313,810 SLC2A12
    nsv6563707inversion1nstd223human GRCh38 chr6: 125,606,968-134,343,906 , GRCh37.p13 chr6: 125,928,114-134,665,044 TAAR2, LOC105377996, 130 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
    nsv6269920copy number variation1nstd214human GRCh38 chr6: 134,032,405-134,032,468 , GRCh37.p13 chr6: 134,353,543-134,353,606 SLC2A12
    nsv6268952copy number variation1nstd214human GRCh38 chr6: 134,032,405-134,032,470 , GRCh37.p13 chr6: 134,353,543-134,353,608 SLC2A12
    nsv6268776copy number variation1nstd214human GRCh38 chr6: 134,032,405-134,032,472 , GRCh37.p13 chr6: 134,353,543-134,353,610 SLC2A12
    nsv6266412copy number variation1nstd214human GRCh38 chr6: 134,032,428-134,032,484 , GRCh37.p13 chr6: 134,353,566-134,353,622 SLC2A12
    nsv6265733copy number variation1nstd214human GRCh38 chr6: 134,032,418-134,032,467 , GRCh37.p13 chr6: 134,353,556-134,353,605 SLC2A12
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