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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4676292copy number variation1nstd102humanPathogenic GRCh37 chr22: 30,654,764-51,197,838 , GRCh38.p12 chr22: 30,258,775-50,759,410 PDXP-DT, PDGFB, 550 more genes
    nsv4630494copy number variation1nstd183human GRCh37 chr22: 37,960,725-37,993,126 , GRCh38.p12 chr22: 37,564,718-37,597,119 LGALS2, CDC42EP1
    nsv4629940copy number variation1nstd183human GRCh37 chr22: 37,956,395-37,956,633 , GRCh38.p12 chr22: 37,560,388-37,560,626 CDC42EP1
    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
    nsv4282683copy number variation1nstd166human GRCh37.p13 chr22: 37,962,283-37,962,340 , GRCh38.p12 chr22: 37,566,276-37,566,333 CDC42EP1
    nsv4278013copy number variation1nstd166human GRCh37.p13 chr22: 37,381,892-38,500,309 , GRCh38.p12 chr22: 36,985,851-38,104,302 GGA1, GALR3, 46 more genes
    nsv3922128copy number variation1nstd102humanPathogenic GRCh37 chr22: 35,729,986-39,296,182 , NCBI36 chr22: 34,059,986-37,626,128 , GRCh38 chr22: 35,333,993-38,900,177 LOC102724378, CARD10, 120 more genes
    nsv3919881copy number variation1nstd102humanPathogenic GRCh37 chr22: 17,397,633-51,178,213 , GRCh38 chr22: 16,916,743-50,739,785 , NCBI36 chr22: 15,777,633-49,525,079 MIR12114, MIR6820, 1059 more genes
    nsv3919085copy number variation1nstd102humanPathogenic NCBI36 chr22: 17,008,132-49,591,432 , GRCh37.p13 chr22: 18,628,132-51,244,566 , GRCh38.p12 chr22: 18,145,365-50,806,138 IGLV2-28, LINC01310, 1023 more genes
    nsv3917356copy number variation1nstd102humanUncertain significance GRCh37 chr22: 37,520,289-37,976,764 , NCBI36 chr22: 35,850,235-36,306,710 , GRCh38 chr22: 37,124,249-37,580,757 C1QTNF6, LOC105373024, 12 more genes
    nsv3915039copy number variation1nstd102humanPathogenic GRCh38 chr22: 37,447,222-39,103,680 , GRCh37 chr22: 37,843,259-39,499,685 , NCBI36 chr22: 36,173,205-37,829,631 MIR4534, SLC16A8, 68 more genes
    nsv3914747copy number variation1nstd102humanPathogenic NCBI36 chr22: 35,278,369-36,395,868 , GRCh38 chr22: 36,552,376-37,669,915 , GRCh37 chr22: 36,948,423-38,065,922 ELFN2, LGALS2, 35 more genes
    nsv3913775copy number variation1nstd102humanPathogenic NCBI36 chr22: 15,777,498-49,525,130 , GRCh38 chr22: 16,916,608-50,739,836 , GRCh37 chr22: 17,397,498-51,178,264 ZNF280A, RFPL1S, 1059 more genes
    nsv3913040copy number variation1nstd102humanUncertain significance NCBI36 chr22: 36,263,270-36,529,310 , GRCh38 chr22: 37,537,317-37,803,357 , GRCh37 chr22: 37,933,324-38,199,364 PDXP-DT, CDC42EP1, 10 more genes
    nsv3910634copy number variation1nstd102humanPathogenic GRCh38 chr22: 37,061,769-50,738,932 , NCBI36 chr22: 35,787,755-49,524,226 , GRCh37 chr22: 37,457,809-51,177,360 HDAC10, RPS25P10, 381 more genes
    nsv3908935copy number variation1nstd102humanBenign GRCh37 chr22: 37,956,214-37,992,704 , GRCh38.p12 chr22: 37,560,207-37,596,697 CDC42EP1, LGALS2
    nsv3907231copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,114,244-51,211,392 , GRCh38.p12 chr22: 16,367,190-50,772,964 DDTL, PPP1R26P3, 1084 more genes
    nsv3906962copy number variation1nstd102humanPathogenic GRCh37 chr22: 35,728,929-51,220,961 , GRCh38.p12 chr22: 35,332,936-50,782,533 UQCRFS1P1, APOBEC3F, 435 more genes
    nsv3904443copy number variation1nstd102humanPathogenic GRCh37 chr22: 36,877,226-38,548,989 , GRCh38.p12 chr22: 36,481,179-38,152,982 LOC107985576, IL2RB, 63 more genes
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