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Items: 1 to 20 of 109

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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
    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
    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
    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
    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
    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
    nsv3924220copy number variation1nstd102humanPathogenic GRCh38 chr12: 115,131,583-133,166,920 , NCBI36 chr12: 114,053,771-132,253,579 , GRCh37 chr12: 115,569,388-133,743,506 LOC105370080, LINC02985, 376 more genes
    nsv3923347copy number variation1nstd102humanPathogenic NCBI36 chr12: 119,619,858-132,289,149 , GRCh37 chr12: 121,135,475-133,779,076 , GRCh38 chr12: 120,697,672-133,202,490 LOC105370044, RNU6-1017P, 273 more genes
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