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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074549inversion1nstd229human GRCh38 chr12: 130,041,403-130,041,434 , GRCh37.p13 chr12: 130,525,948-130,525,979 LINC02418
    nsv7074199inversion1nstd229human GRCh38 chr12: 123,186,434-132,825,682 , GRCh37.p13 chr12: 123,670,981-133,402,268 PIWIL1, FZD10-AS1, 187 more genes
    nsv7072492inversion1nstd229human GRCh38 chr12: 129,800,433-131,135,675 , GRCh37.p13 chr12: 130,284,978-131,620,220 TMEM132D, LOC105370077, 17 more genes
    nsv7065233inversion1nstd229human GRCh38 chr12: 129,874,079-131,069,710 , GRCh37.p13 chr12: 130,358,624-131,554,255 RAN, STX2, 16 more genes
    nsv7059834inversion1nstd229human GRCh38 chr12: 129,800,267-131,126,796 , GRCh37.p13 chr12: 130,284,812-131,611,341 ADGRD1-AS1, RAN, 17 more genes
    nsv6933567copy number variation1nstd229human GRCh38 chr12: 129,285,987-130,239,345 , GRCh37.p13 chr12: 129,770,532-130,723,890 LOC105370076, FZD10, 7 more genes
    nsv6930440copy number variation1nstd229human GRCh38 chr12: 130,042,377-130,057,849 , GRCh37.p13 chr12: 130,526,922-130,542,394 LINC02418
    nsv6930371copy number variation1nstd229human GRCh38 chr12: 129,871,346-130,315,342 , GRCh37.p13 chr12: 130,355,891-130,799,887 FZD10, LOC105370076, 7 more genes
    nsv6576184inversion1nstd223human GRCh38 chr12: 130,022,299-130,256,753 , GRCh37.p13 chr12: 130,506,844-130,741,298 FZD10, FZD10-AS1, 4 more genes
    nsv6487263copy number variation1nstd223human GRCh38 chr12: 129,871,346-130,315,340 , GRCh37.p13 chr12: 130,355,891-130,799,885 TMEM132D, LINC02419, 7 more genes
    nsv6290239copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 117,461,902-133,841,395 , GRCh38.p12 chr12: 117,024,097-133,264,809 ACADS, BCL7A, 356 more genes
    nsv6132147copy number variation1nstd213human GRCh37 chr12: 130,350,000-130,750,001 , GRCh38.p12 chr12: 129,865,455-130,265,456 FZD10, TMEM132D, 6 more genes
    nsv5494141copy number variation1nstd206human GRCh38 chr12: 129,527,330-130,603,455 , GRCh37.p13 chr12: 130,011,875-131,088,000 LINC02419, RIMBP2, 10 more genes
    nsv4729329copy number variation1nstd102humanLikely benign GRCh37 chr12: 130,192,184-131,023,667 , GRCh38.p12 chr12: 129,707,639-130,539,122 RPS20P30, FZD10, 10 more genes
    nsv4646444copy number variation1nstd186human GRCh37 chr12: 130,402,334-130,582,861 , GRCh38.p12 chr12: 129,917,789-130,098,316 LINC02418, LOC105370076, 2 more genes
    nsv4456888copy number variation1nstd102humanUncertain significance GRCh37 chr12: 126,470,636-133,777,902 , GRCh38.p12 chr12: 125,986,090-133,201,316 LINC02347, LOC107987176, 145 more genes
    nsv4421515copy number variation1nstd174human GRCh37 chr12: 130,518,109-130,518,541 , GRCh38.p12 chr12: 130,033,564-130,033,996 LINC02418
    nsv4416499copy number variation1nstd174human GRCh37 chr12: 130,423,119-130,718,971 , GRCh38.p12 chr12: 129,938,574-130,234,426 FZD10, FZD10-AS1, 5 more genes
    nsv4349911copy number variation1nstd102humanPathogenic GRCh37 chr12: 125,451,405-133,810,935 , GRCh38.p12 chr12: 124,966,859-133,234,349 LOC107987177, GOLGA3, 159 more genes
    nsv3947777copy number variation1nstd167human GRCh37 chr12: 130,518,305-130,518,346 , GRCh38.p12 chr12: 130,033,760-130,033,801 LINC02418
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