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Items: 1 to 20 of 602

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148281copy number variation1nstd102humanPathogenic GRCh38 chr22: 49,757,859-50,740,457 , GRCh37.p13 chr22: 50,151,507-51,178,885 CHKB-CPT1B, ADM2, 49 more genes
    nsv7148150copy number variation1nstd102humanPathogenic GRCh37 chr22: 50,014,114-51,244,066 , GRCh38.p12 chr22: 49,620,466-50,805,638 MAPK11, KLHDC7B-DT, 54 more genes
    nsv7144478copy number variation1nstd232human GRCh37.p13 chr22: 50,499,126-50,499,227 , GRCh38.p12 chr22: 50,060,697-50,060,798 MLC1
    nsv7143924copy number variation1nstd232human GRCh37.p13 chr22: 50,520,603-50,520,664 , GRCh38.p12 chr22: 50,082,174-50,082,235 MLC1
    nsv7140223insertion1nstd232human GRCh37.p13 chr22: 50,511,475-50,511,475 , GRCh38.p12 chr22: 50,073,046-50,073,046 MLC1
    nsv7137953copy number variation1nstd232human GRCh37.p13 chr22: 50,499,188-50,499,238 , GRCh38.p12 chr22: 50,060,759-50,060,809 MLC1
    nsv7096318copy number variation1nstd102humanPathogenic GRCh37 chr22: 50,518,954-50,523,273 , GRCh38.p12 chr22: 50,080,525-50,084,844 MLC1
    nsv7096317copy number variation1nstd102humanUncertain significance GRCh37 chr22: 50,512,625-50,523,373 , GRCh38.p12 chr22: 50,074,196-50,084,944 MLC1
    nsv7096316copy number variation1nstd102humanPathogenic GRCh37 chr22: 50,297,486-51,066,207 , GRCh38.p12 chr22: 49,903,838-50,627,779 RN7SL500P, DENND6B, 39 more genes
    nsv7096187copy number variation1nstd102humanPathogenic GRCh37 chr22: 50,523,145-50,523,373 , GRCh38.p12 chr22: 50,084,716-50,084,944 MLC1
    nsv7096186copy number variation1nstd102humanUncertain significance GRCh37 chr22: 50,515,250-50,515,951 , GRCh38.p12 chr22: 50,076,821-50,077,522 MLC1
    nsv7096185copy number variation1nstd102humanPathogenic GRCh37 chr22: 50,500,012-50,515,951 , GRCh38.p12 chr22: 50,061,583-50,077,522 MLC1
    nsv7096184copy number variation1nstd102humanPathogenic GRCh37 chr22: 50,500,002-50,523,373 , GRCh38.p12 chr22: 50,061,573-50,084,944 MLC1
    nsv7033075copy number variation1nstd229human GRCh38 chr22: 49,877,724-50,553,749 , GRCh37.p13 chr22: 50,271,372-50,992,178 SELENOO-AS1, MOV10L1, 33 more genes
    nsv7033048copy number variation1nstd229human GRCh38 chr22: 50,073,156-50,093,624 , GRCh37.p13 chr22: 50,511,585-50,532,053 MLC1, MOV10L1
    nsv7031449copy number variation1nstd229human GRCh38 chr22: 50,006,398-50,235,771 , GRCh37.p13 chr22: 50,444,827-50,674,200 PANX2, SELENOO-AS1, 7 more genes
    nsv7029174copy number variation1nstd229human GRCh38 chr22: 50,065,820-50,068,887 , GRCh37.p13 chr22: 50,504,249-50,507,316 MLC1
    nsv7026590copy number variation1nstd229human GRCh38 chr22: 50,077,366-50,077,503 , GRCh37.p13 chr22: 50,515,795-50,515,932 MLC1
    nsv7025046copy number variation1nstd229human GRCh38 chr22: 50,062,659-50,120,705 , GRCh37.p13 chr22: 50,501,088-50,559,134 MLC1, MOV10L1
    nsv7024318copy number variation1nstd229human GRCh38 chr22: 50,053,362-50,057,504 , GRCh37.p13 chr22: 50,491,791-50,495,933 MLC1, TTLL8
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