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Items: 1 to 20 of 180

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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
    nsv6812686copy number variation1nstd229human GRCh38 chr6: 133,968,641-133,972,401 , GRCh37.p13 chr6: 134,289,779-134,293,539 TBPL1
    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
    nsv6567814inversion1nstd223human GRCh38 chr6: 133,963,406-133,964,071 , GRCh37.p13 chr6: 134,284,544-134,285,209 TBPL1
    nsv6563707inversion1nstd223human GRCh38 chr6: 125,606,968-134,343,906 , GRCh37.p13 chr6: 125,928,114-134,665,044 TAAR2, LOC105377996, 130 more genes
    nsv6303580copy number variation1nstd186human GRCh37 chr6: 134,289,779-134,293,534 , GRCh38.p12 chr6: 133,968,641-133,972,396 TBPL1
    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
    nsv6257222mobile element insertion1nstd215human GRCh38 chr6: 133,985,488-133,985,488 , GRCh37.p13 chr6: 134,306,626-134,306,626 TBPL1
    nsv6136169copy number variation1nstd213human GRCh37 chr6: 133,310,000-134,340,001 , GRCh38.p12 chr6: 132,988,861-134,018,863 EYA4, TCF21, 10 more genes
    nsv6112726copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,810,210-140,046,615 , GRCh38.p12 chr6: 133,489,072-139,725,478 SIMALR, MTFR2, 99 more genes
    nsv5968494inversion1nstd209human GRCh38 chr6: 125,606,968-134,343,905 , GRCh37.p13 chr6: 125,928,114-134,665,043 , ARG1, 137 more genes
    nsv5959255insertion1nstd209human GRCh38 chr6: 133,987,647-133,987,647 , GRCh37.p13 chr6: 134,308,785-134,308,785 SLC2A12, TBPL1
    nsv5685902mobile element insertion2nstd211human GRCh38 chr6: 133,990,918-133,990,918 , GRCh37.p13 chr6: 134,312,056-134,312,056 SLC2A12, TBPL1
    nsv5680035mobile element insertion1nstd211human GRCh38 chr6: 133,960,436-133,960,436 , GRCh37.p13 chr6: 134,281,574-134,281,574 TBPL1
    nsv5467619copy number variation1nstd206human GRCh38 chr6: 133,968,641-133,972,396 , GRCh37.p13 chr6: 134,289,779-134,293,534 TBPL1
    nsv5467293copy number variation1nstd206human GRCh38 chr6: 133,984,239-133,986,506 , GRCh37.p13 chr6: 134,305,377-134,307,644 TBPL1, SLC2A12
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