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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073094inversion1nstd229human GRCh38 chr22: 22,618,607-30,089,219 , GRCh37.p13 chr22: 22,961,077-30,485,208 BCRP1, POM121L10P, 237 more genes
    nsv7068065inversion1nstd229human GRCh38 chr22: 27,585,838-32,538,391 , GRCh37.p13 chr22: 27,981,799-32,934,377 LOC105372995, NEFH, 147 more genes
    nsv7065500inversion1nstd229human GRCh38 chr22: 29,260,563-37,652,385 , GRCh37.p13 chr22: 29,656,552-38,048,392 RFPL1, PATZ1, 217 more genes
    nsv7028628copy number variation1nstd229human GRCh38 chr22: 29,261,801-29,266,300 , GRCh37.p13 chr22: 29,657,790-29,662,289 EWSR1, RHBDD3
    nsv7019517copy number variation1nstd229human GRCh38 chr22: 29,258,401-29,265,800 , GRCh37.p13 chr22: 29,654,390-29,661,789 EMID1, RHBDD3
    nsv6637977copy number variation1nstd102humanPathogenic GRCh37 chr22: 26,614,429-29,847,680 , GRCh38.p12 chr22: 26,218,463-29,451,691 MIAT, LOC105372985, 65 more genes
    nsv6311263copy number variation1nstd102humanUncertain significance GRCh37 chr22: 29,083,885-34,046,674 , GRCh38.p12 chr22: 28,687,897-33,650,688 SNORD125, LOC107985533, 145 more genes
    nsv6146556copy number variation1nstd206human GRCh38 chr22: 29,263,330-29,263,428 , GRCh37.p13 chr22: 29,659,319-29,659,417 RHBDD3
    nsv6134119copy number variation1nstd213human GRCh37 chr22: 29,540,000-30,070,001 , GRCh38.p12 chr22: 29,144,012-29,674,012 AP1B1, EWSR1, 19 more genes
    nsv6134118copy number variation1nstd213human GRCh37 chr22: 27,870,000-35,640,001 , GRCh38.p12 chr22: 27,474,039-35,244,008 AP1B1, EWSR1, 172 more genes
    nsv6134111copy number variation1nstd213human GRCh37 chr22: 29,604,611-29,815,875 , GRCh38.p12 chr22: 29,208,622-29,419,886 RASL10A, EMID1, 8 more genes
    nsv5673427copy number variation1nstd102humanPathogenic GRCh37 chr22: 29,083,885-30,337,586 , GRCh38.p12 chr22: 28,687,897-29,941,597 SNORD125, RASL10A, 36 more genes
    nsv5673351copy number variation1nstd102humanPathogenic GRCh37 chr22: 29,105,984-30,337,586 , GRCh38.p12 chr22: 28,709,996-29,941,597 SNORD125, RASL10A, 36 more genes
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4729897copy number variation1nstd102humanPathogenic GRCh37 chr22: 28,291,202-30,450,920 , GRCh38.p12 chr22: 27,895,214-30,054,931 RNU6-810P, THOC5, 48 more genes
    nsv4683866copy number variation1nstd102humanPathogenic GRCh37 chr22: 29,083,875-30,090,801 , GRCh38.p12 chr22: 28,687,887-29,694,812 RNU6-1219P, EMID1, 29 more genes
    nsv4621467copy number variation1nstd183human GRCh37 chr22: 29,663,786-29,664,190 , GRCh38.p12 chr22: 29,267,797-29,268,201 EWSR1, RHBDD3
    nsv4457771copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410 IGLV3-27, XKR3, 1082 more genes
    nsv4383389copy number variation1nstd173human GRCh37 chr22: 21,465,662-33,984,045 , GRCh38.p12 chr22: 21,111,373-33,588,059 , XBP1, 450 more genes
    nsv4316382inversion1nstd166human GRCh37.p13 chr22: 22,466,414-30,881,792 , GRCh38.p12 chr22: 22,112,004-30,485,805 , CRYBB2, 313 more genes
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