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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
    nsv7096188copy number variation1nstd102humanPathogenic GRCh37 chr22: 50,659,287-50,697,352 , GRCh38.p12 chr22: 50,220,858-50,258,923 MAPK12, TUBGCP6, 1 more genes
    nsv3893588copy number variation1nstd102humanBenign GRCh37 chr22: 50,682,728-50,724,648 , GRCh38.p12 chr22: 50,244,299-50,286,219 MAPK12, PLXNB2, 3 more genes
    nsv3907079copy number variation1nstd102humanBenign GRCh37 chr22: 50,684,747-50,724,648 , GRCh38.p12 chr22: 50,246,318-50,286,219 MAPK12, HDAC10, 2 more genes
    nsv3903193copy number variation1nstd102humanBenign GRCh37 chr22: 50,684,771-50,724,504 , GRCh38.p12 chr22: 50,246,342-50,286,075 MAPK12, HDAC10, 2 more genes
    nsv3906203copy number variation1nstd102humanBenign GRCh37 chr22: 50,684,772-50,721,495 , GRCh38.p12 chr22: 50,246,343-50,283,066 MAPK12, HDAC10, 2 more genes
    nsv3893151copy number variation1nstd102humanBenign GRCh37 chr22: 50,688,348-50,721,495 , GRCh38.p12 chr22: 50,249,919-50,283,066 MAPK12, PLXNB2, 2 more genes
    nsv3894798copy number variation1nstd102humanBenign GRCh37 chr22: 50,697,119-50,715,271 , GRCh38.p12 chr22: 50,258,690-50,276,842 MAPK12, PLXNB2, 1 more genes
    nsv3906388copy number variation1nstd102humanBenign GRCh37 chr22: 50,699,625-50,714,616 , GRCh38.p12 chr22: 50,261,196-50,276,187 MAPK12, MAPK11, 1 more genes
    nsv3895794copy number variation1nstd102humanBenign GRCh37 chr22: 50,699,625-50,713,409 , GRCh38.p12 chr22: 50,261,196-50,274,980 MAPK12, MAPK11, 1 more genes
    nsv4683870copy number variation1nstd102humanUncertain significance GRCh37 chr22: 50,664,223-50,694,310 , GRCh38.p12 chr22: 50,225,794-50,255,881 MAPK12, TUBGCP6, 1 more genes
    nsv3900214copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,151,555-51,195,728 , GRCh38.p12 chr22: 41,755,551-50,757,300 MAPK12, TYMP, 218 more genes
    nsv6290298copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,321,321-51,244,066 , GRCh38.p12 chr22: 41,925,317-50,805,638 MAPK12, CERK, 212 more genes
    nsv3912011copy number variation1nstd102humanPathogenic NCBI36 chr22: 40,597,093-49,525,130 , GRCh38 chr22: 41,871,143-50,739,836 , GRCh37 chr22: 42,267,147-51,178,264 MAPK12, TUBGCP6, 213 more genes
    nsv5381149copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,333,802-51,195,728 , GRCh38.p12 chr22: 41,937,798-50,757,300 MAPK12, WBP2NL, 210 more genes
    nsv4351202copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,416,026-51,181,759 , GRCh38.p12 chr22: 42,020,022-50,743,331 MAPK12, PLXNB2, 204 more genes
    nsv3893572copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,441,918-51,197,838 , GRCh38.p12 chr22: 42,045,914-50,759,410 MAPK12, CYP2D8P, 206 more genes
    nsv3920027copy number variation1nstd102humanPathogenic GRCh38 chr22: 42,433,752-50,738,932 , NCBI36 chr22: 41,159,702-49,524,226 , GRCh37 chr22: 42,829,758-51,177,360 MAPK12, MIR6821, 187 more genes
    nsv3909355copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,955,616-51,183,840 , GRCh38.p12 chr22: 42,559,610-50,745,412 MAPK12, LOC101927499, 182 more genes
    nsv6314059copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,972,719-51,197,838 , GRCh38.p12 chr22: 42,576,713-50,759,410 MAPK12, TRABD, 181 more genes
    nsv3897841copy number variation1nstd102humanPathogenic GRCh37 chr22: 43,050,743-51,197,838 , GRCh38.p12 chr22: 42,654,737-50,759,410 MAPK12, LINC00229, 176 more genes
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