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Items: 1 to 20 of 1378

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131253insertion1nstd186human GRCh37 chr12: 128,949,341-128,949,386 , GRCh38.p12 chr12: 128,464,796-128,464,841 TMEM132C
    nsv6131214insertion1nstd186human GRCh37 chr12: 128,967,868-128,967,875 , GRCh38.p12 chr12: 128,483,323-128,483,330 TMEM132C
    nsv6130359insertion1nstd186human GRCh37 chr12: 128,989,553-128,989,564 , GRCh38.p12 chr12: 128,505,008-128,505,019 TMEM132C
    nsv6129909mobile element insertion1nstd186human GRCh37 chr12: 128,777,557-128,777,608 , GRCh38.p12 chr12: 128,293,012-128,293,063 TMEM132C, MIR3612
    nsv6123022copy number variation1nstd186human GRCh37 chr12: 129,132,269-129,132,720 , GRCh38.p12 chr12: 128,647,724-128,648,175 TMEM132C
    nsv6122136copy number variation1nstd186human GRCh37 chr12: 128,932,255-128,932,541 , GRCh38.p12 chr12: 128,447,710-128,447,996 TMEM132C
    nsv6121084copy number variation1nstd186human GRCh37 chr12: 129,192,734-129,192,984 , GRCh38.p12 chr12: 128,708,189-128,708,439 TMEM132C
    nsv6114442mobile element insertion1nstd186human GRCh37 chr12: 128,933,918-128,933,969 , GRCh38.p12 chr12: 128,449,373-128,449,424 TMEM132C
    nsv5979492insertion1nstd209human GRCh38 chr12: 128,686,057-128,686,057 , GRCh37.p13 chr12: 129,170,602-129,170,602 TMEM132C
    nsv5979266insertion1nstd209human GRCh38 chr12: 128,292,999-128,292,999 , GRCh37.p13 chr12: 128,777,544-128,777,544 TMEM132C, MIR3612
    nsv5978537insertion1nstd209human GRCh38 chr12: 128,504,968-128,504,968 , GRCh37.p13 chr12: 128,989,513-128,989,513 TMEM132C
    nsv5978062insertion1nstd209human GRCh38 chr12: 128,566,189-128,566,189 , GRCh37.p13 chr12: 129,050,734-129,050,734 TMEM132C
    nsv5975340insertion1nstd209human GRCh38 chr12: 128,626,445-128,626,445 , GRCh37.p13 chr12: 129,110,990-129,110,990 TMEM132C
    nsv5969907insertion1nstd209human GRCh38 chr12: 128,464,790-128,464,790 , GRCh37.p13 chr12: 128,949,335-128,949,335 TMEM132C
    nsv5969815insertion1nstd209human GRCh38 chr12: 128,473,334-128,473,334 , GRCh37.p13 chr12: 128,957,879-128,957,879 TMEM132C
    nsv5946221copy number variation1nstd209human GRCh38 chr12: 128,647,689-128,648,279 , GRCh37.p13 chr12: 129,132,234-129,132,824 TMEM132C
    nsv5945417copy number variation1nstd209human GRCh38 chr12: 128,572,231-128,572,324 , GRCh37.p13 chr12: 129,056,776-129,056,869 TMEM132C
    nsv5943210copy number variation1nstd209human GRCh38 chr12: 128,593,138-128,593,313 , GRCh37.p13 chr12: 129,077,683-129,077,858 TMEM132C
    nsv5942476copy number variation1nstd209human GRCh38 chr12: 128,648,825-128,649,063 , GRCh37.p13 chr12: 129,133,370-129,133,608 TMEM132C
    nsv5940433copy number variation1nstd209human GRCh38 chr12: 128,473,168-128,473,383 , GRCh37.p13 chr12: 128,957,713-128,957,928 TMEM132C
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