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Items: 1 to 20 of 334

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116876mobile element insertion1nstd186human GRCh37 chr2: 231,982,838-231,982,838 , GRCh38.p12 chr2: 231,118,124-231,118,124 PSMD1, HTR2B
    nsv5959112insertion1nstd209human GRCh38 chr2: 231,118,124-231,118,124 , GRCh37.p13 chr2: 231,982,838-231,982,838 PSMD1, HTR2B
    nsv5900395copy number variation1nstd209human GRCh38 chr2: 231,093,089-231,093,164 , GRCh37.p13 chr2: 231,957,803-231,957,878 PSMD1
    nsv5897084copy number variation1nstd209human GRCh38 chr2: 231,053,804-231,055,685 , GRCh37.p13 chr2: 231,918,518-231,920,399 PSMD1, LOC112268432
    nsv5894046copy number variation1nstd209human GRCh38 chr2: 231,105,479-231,106,801 , GRCh37.p13 chr2: 231,970,193-231,971,515 HTR2B, PSMD1
    nsv5888105copy number variation1nstd209human GRCh38 chr2: 231,131,462-231,131,785 , GRCh37.p13 chr2: 231,996,176-231,996,499 RNU1-93P, PSMD1
    nsv5832543copy number variation1nstd209human GRCh38 chr2: 231,105,804-231,106,803 , GRCh37.p13 chr2: 231,970,518-231,971,517 PSMD1, HTR2B
    nsv5832239copy number variation1nstd209human GRCh38 chr2: 231,053,794-231,055,793 , GRCh37.p13 chr2: 231,918,508-231,920,507 PSMD1, LOC112268432
    nsv5679775mobile element insertion2nstd211human GRCh38 chr2: 231,118,139-231,118,139 , GRCh37.p13 chr2: 231,982,853-231,982,853 PSMD1, HTR2B
    nsv5616061insertion1nstd207human GRCh38 chr2: 231,118,124-231,118,124 , GRCh37.p13 chr2: 231,982,838-231,982,838 PSMD1, HTR2B
    nsv5579419copy number variation1nstd207human GRCh38 chr2: 231,165,024-231,165,077 , GRCh37.p13 chr2: 232,029,738-232,029,791 PSMD1
    nsv5565158copy number variation1nstd207human GRCh38 chr2: 231,131,462-231,131,785 , GRCh37.p13 chr2: 231,996,176-231,996,499 RNU1-93P, PSMD1
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5556423sequence alteration1nstd206human GRCh38 chr2: 231,166,199-231,166,205 , GRCh37.p13 chr2: 232,030,913-232,030,919 PSMD1
    nsv5451766copy number variation1nstd206human GRCh38 chr2: 231,076,383-231,076,472 , GRCh37.p13 chr2: 231,941,097-231,941,186 PSMD1
    nsv5451647copy number variation1nstd206human GRCh38 chr2: 231,053,807-231,055,686 , GRCh37.p13 chr2: 231,918,521-231,920,400 PSMD1, LOC112268432
    nsv5449507copy number variation1nstd206human GRCh38 chr2: 231,081,132-231,081,191 , GRCh37.p13 chr2: 231,945,846-231,945,905 PSMD1
    nsv5448639copy number variation1nstd206human GRCh38 chr2: 231,088,055-231,088,579 , GRCh37.p13 chr2: 231,952,769-231,953,293 PSMD1
    nsv5446950copy number variation1nstd206human GRCh38 chr2: 231,153,282-231,153,349 , GRCh37.p13 chr2: 232,017,996-232,018,063 PSMD1
    nsv5445664copy number variation1nstd206human GRCh38 chr2: 231,080,941-231,082,476 , GRCh37.p13 chr2: 231,945,655-231,947,190 PSMD1
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