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Items: 1 to 20 of 124

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054895inversion1nstd229human GRCh38 chr2: 229,787,965-232,576,060 , GRCh37.p13 chr2: 230,652,681-233,440,770 GPR55, RN7SL834P, 80 more genes
    nsv6697310copy number variation1nstd229human GRCh38 chr2: 231,016,947-231,455,744 , GRCh37.p13 chr2: 231,881,662-232,320,455 B3GNT7, RPS28P4, 13 more genes
    nsv6691023copy number variation1nstd229human GRCh38 chr2: 231,095,700-231,107,144 , GRCh37.p13 chr2: 231,960,414-231,971,858 HTR2B, PSMD1
    nsv6546539inversion1nstd223human GRCh38 chr2: 231,119,599-231,120,128 , GRCh37.p13 chr2: 231,984,313-231,984,842 HTR2B, PSMD1
    nsv6543239inversion1nstd223human GRCh38 chr2: 231,119,599-231,120,124 , GRCh37.p13 chr2: 231,984,313-231,984,838 PSMD1, HTR2B
    nsv6341797copy number variation1nstd223human GRCh38 chr2: 231,121,501-231,123,000 , GRCh37.p13 chr2: 231,986,215-231,987,714 HTR2B, PSMD1
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313683copy number variation1nstd102humanPathogenic GRCh37 chr2: 228,807,574-235,475,892 , GRCh38.p12 chr2: 227,942,858-234,567,248 RNU7-9P, SCARNA5, 143 more genes
    nsv6313668copy number variation1nstd102humanPathogenic GRCh37 chr2: 219,606,537-239,217,703 , GRCh38.p12 chr2: 218,741,814-238,309,062 LOC105373947, RN7SL764P, 357 more genes
    nsv6311650copy number variation2nstd102humanUncertain significance GRCh37 chr2: 231,033,840-234,978,657 , GRCh38.p12 chr2: 230,169,124-234,070,013 SP110, LINC00471, 112 more genes
    nsv6134539copy number variation1nstd213human GRCh37 chr2: 231,850,000-233,400,001 , GRCh38.p12 chr2: 230,985,285-232,535,291 ALPI, ALPP, 47 more genes
    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
    nsv5894046copy number variation1nstd209human GRCh38 chr2: 231,105,479-231,106,801 , GRCh37.p13 chr2: 231,970,193-231,971,515 HTR2B, PSMD1
    nsv5832543copy number variation1nstd209human GRCh38 chr2: 231,105,804-231,106,803 , GRCh37.p13 chr2: 231,970,518-231,971,517 PSMD1, HTR2B
    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
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5436095copy number variation1nstd206human GRCh38 chr2: 231,118,287-231,118,382 , GRCh37.p13 chr2: 231,983,001-231,983,096 HTR2B, PSMD1
    nsv5400217mobile element insertion1nstd206human GRCh38 chr2: 231,118,124-231,118,124 , GRCh37.p13 chr2: 231,982,838-231,982,838 HTR2B, PSMD1
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