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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096653copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,121,051-47,710,088 , GRCh38.p12 chr2: 37,893,908-47,482,949 PLEKHH2, RNU6-566P, 151 more genes
    nsv7039759inversion1nstd229human GRCh38 chr2: 39,986,388-47,339,194 , GRCh37.p13 chr2: 40,213,528-47,566,333 RPL36AP14, CRIPT, 105 more genes
    nsv6658391copy number variation1nstd229human GRCh38 chr2: 42,288,901-43,411,600 , GRCh37.p13 chr2: 42,516,041-43,638,739 LOC112268413, RNU6-958P, 22 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6134459copy number variation1nstd213human GRCh37 chr2: 40,080,000-50,820,001 , GRCh38.p12 chr2: 39,852,860-50,592,863 , BCYRN1, 149 more genes
    nsv6134458copy number variation2nstd213human GRCh37 chr2: 38,440,000-47,670,001 , GRCh38.p12 chr2: 38,212,858-47,442,862 ASS1P2, BCYRN1, 144 more genes
    nsv6134457copy number variation1nstd213human GRCh37 chr2: 38,410,000-75,540,001 , GRCh38.p12 chr2: 38,182,858-75,312,875 , ACTG2, 598 more genes
    nsv6112680copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 24,881,528-43,460,021 , GRCh38.p12 chr2: 24,658,659-43,232,882 ADCY3, ALK, 314 more genes
    nsv4679262copy number variation1nstd189human GRCh38.p12 chr2: 43,209,612-43,481,258 , GRCh37.p13 chr2: 43,436,751-43,708,397 , ZFP36L2, 3 more genes
    nsv4595583copy number variation1nstd183human GRCh37 chr2: 43,450,114-43,456,040 , GRCh38.p12 chr2: 43,222,975-43,228,901 LINC01126, ZFP36L2, 1 more genes
    nsv4586054copy number variation1nstd183human GRCh37 chr2: 43,451,425-43,454,915 , GRCh38.p12 chr2: 43,224,286-43,227,776 ZFP36L2, LINC01126
    nsv4586053copy number variation1nstd183human GRCh37 chr2: 43,335,867-43,503,569 , GRCh38.p12 chr2: 43,108,728-43,276,430 , THADA, 3 more genes
    nsv4402791copy number variation1nstd174human GRCh37 chr2: 43,450,138-43,455,109 , GRCh38.p12 chr2: 43,222,999-43,227,970 ZFP36L2, LINC01126
    nsv4398598copy number variation1nstd174human GRCh37 chr2: 43,450,138-43,454,915 , GRCh38.p12 chr2: 43,222,999-43,227,776 LINC01126, ZFP36L2
    nsv4335876sequence alteration1nstd166human GRCh37.p13 chr2: 20,021,666-53,788,063 , GRCh38.p12 chr2: 19,821,905-53,560,926 , ADCY3, 531 more genes
    nsv4331174inversion1nstd166human GRCh37.p13 chr2: 36,139,982-53,112,348 , GRCh38.p12 chr2: 35,914,916-52,885,210 , ASS1P2, 247 more genes
    nsv3919677inversion1nstd102humanPathogenic GRCh38.p12 chr2: 37,893,967-47,442,383 , GRCh37 chr2: 38,121,110-47,669,522 ASS1P2, BCYRN1, 151 more genes
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