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Items: 1 to 20 of 195

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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
    nsv6817223copy number variation1nstd229human GRCh38 chr6: 132,757,601-132,762,700 , GRCh37.p13 chr6: 133,078,740-133,083,839 VNN2, RBM11P1
    nsv6816420copy number variation1nstd229human GRCh38 chr6: 132,749,116-132,753,796 , GRCh37.p13 chr6: 133,070,255-133,074,935 VNN2
    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
    nsv6809931copy number variation1nstd229human GRCh38 chr6: 132,740,701-132,751,600 , GRCh37.p13 chr6: 133,061,840-133,072,739 VNN2
    nsv6807941copy number variation1nstd229human GRCh38 chr6: 132,754,696-132,762,317 , GRCh37.p13 chr6: 133,075,835-133,083,456 VNN2
    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
    nsv6805115copy number variation1nstd229human GRCh38 chr6: 132,736,590-132,759,774 , GRCh37.p13 chr6: 133,057,729-133,080,913 VNN2
    nsv6804728copy number variation1nstd229human GRCh38 chr6: 132,753,801-132,772,197 , GRCh37.p13 chr6: 133,074,940-133,093,336 VNN2, RBM11P1, 1 more genes
    nsv6804558copy number variation1nstd229human GRCh38 chr6: 132,745,101-132,750,400 , GRCh37.p13 chr6: 133,066,240-133,071,539 VNN2
    nsv6803637copy number variation1nstd229human GRCh38 chr6: 132,753,001-132,756,000 , GRCh37.p13 chr6: 133,074,140-133,077,139 VNN2
    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
    nsv6618434copy number variation1nstd223human GRCh38 chr6: 132,745,086-132,750,348 , GRCh37.p13 chr6: 133,066,225-133,071,487 VNN2
    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
    nsv6606533copy number variation1nstd223human GRCh38 chr6: 132,736,590-132,759,774 , GRCh37.p13 chr6: 133,057,729-133,080,913 VNN2
    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
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