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Items: 1 to 20 of 154

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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
    nsv7035412copy number variation1nstd229human GRCh38 chr22: 29,066,363-29,073,214 , GRCh37.p13 chr22: 29,462,351-29,469,202 KREMEN1, C22orf31
    nsv7030967copy number variation1nstd229human GRCh38 chr22: 29,063,451-29,065,106 , GRCh37.p13 chr22: 29,459,439-29,461,094 C22orf31
    nsv7019823copy number variation1nstd229human GRCh38 chr22: 29,061,472-29,065,062 , GRCh37.p13 chr22: 29,457,460-29,461,050 C22orf31
    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
    nsv6554819copy number variation1nstd223human GRCh38 chr22: 29,056,350-29,061,462 , GRCh37.p13 chr22: 29,452,338-29,457,450 C22orf31, ZNRF3
    nsv6552122copy number variation1nstd223human GRCh38 chr22: 29,061,492-29,065,044 , GRCh37.p13 chr22: 29,457,480-29,461,032 C22orf31
    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
    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
    nsv6134117copy number variation1nstd213human GRCh37 chr22: 27,870,000-29,490,001 , GRCh38.p12 chr22: 27,474,039-29,094,013 MN1, XBP1, 20 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
    nsv5536885copy number variation1nstd206human GRCh38 chr22: 29,072,800-29,097,674 , GRCh37.p13 chr22: 29,468,788-29,493,662 KREMEN1, C22orf31
    nsv5535803copy number variation1nstd206human GRCh38 chr22: 29,061,462-29,065,073 , GRCh37.p13 chr22: 29,457,450-29,461,061 C22orf31
    nsv5360483translocation1nstd200human GRCh38 chr22: 29,061,492-29,061,492 , GRCh38 chr22: 29,065,044-29,065,044 , GRCh37.p13 chr22: 29,461,032-29,461,032 , GRCh37.p13 chr22: 29,457,480-29,457,480 C22orf31
    nsv5344172translocation1nstd200human GRCh37 chr22: 29,457,480-29,457,480 , GRCh37 chr22: 29,461,032-29,461,032 , GRCh38.p12 chr22: 29,061,492-29,061,492 , GRCh38.p12 chr22: 29,065,044-29,065,044 C22orf31
    nsv5041322copy number variation1nstd200human GRCh38 chr22: 29,065,788-29,066,639 , GRCh37.p13 chr22: 29,461,776-29,462,627 C22orf31
    nsv5038225copy number variation1nstd200human GRCh38 chr22: 29,056,348-29,061,464 , GRCh37.p13 chr22: 29,452,336-29,457,452 ZNRF3, C22orf31
    nsv4854212copy number variation1nstd200human GRCh37 chr22: 29,461,776-29,462,627 , GRCh38.p12 chr22: 29,065,788-29,066,639 C22orf31
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