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Items: 1 to 20 of 141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6930696copy number variation1nstd229human GRCh38 chr12: 130,145,859-130,152,789 , GRCh37.p13 chr12: 130,630,404-130,637,334 FZD10-AS1
    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
    nsv6919671copy number variation1nstd229human GRCh38 chr12: 130,157,701-130,167,900 , GRCh37.p13 chr12: 130,642,246-130,652,445 FZD10-AS1, FZD10
    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
    nsv6132415copy number variation1nstd213human GRCh37 chr12: 130,540,000-132,700,001 , GRCh38.p12 chr12: 130,055,455-132,215,456 ULK1, DDX51, 47 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
    nsv6031686copy number variation1nstd212human GRCh38 chr12: 130,157,738-130,157,792 , GRCh37.p13 chr12: 130,642,283-130,642,337 FZD10-AS1
    nsv5860111copy number variation1nstd209human GRCh38 chr12: 130,157,089-130,160,291 , GRCh37.p13 chr12: 130,641,634-130,644,836 FZD10-AS1
    nsv5600643copy number variation1nstd207human GRCh38 chr12: 130,157,786-130,157,835 , GRCh37.p13 chr12: 130,642,331-130,642,380 FZD10-AS1
    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
    nsv5276501copy number variation1nstd204human GRCh38.p13 chr12: 130,054,901-130,248,200 , GRCh37.p13 chr12: 130,539,446-130,732,745 LOC105370077, LINC02419, 3 more genes
    nsv4747794copy number variation1nstd199human GRCh37 chr12: 130,642,256-130,642,324 , GRCh38.p12 chr12: 130,157,711-130,157,779 FZD10-AS1
    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
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