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Items: 1 to 20 of 1438

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv5966287insertion1nstd209human GRCh38 chr2: 32,959,572-32,959,572 , GRCh37.p13 chr2: 33,184,639-33,184,639 LTBP1
    nsv5961996insertion1nstd209human GRCh38 chr2: 33,182,672-33,182,672 , GRCh37.p13 chr2: 33,407,739-33,407,739 LTBP1
    nsv5960070insertion1nstd209human GRCh38 chr2: 33,006,695-33,006,695 , GRCh37.p13 chr2: 33,231,762-33,231,762 LTBP1
    nsv5959742insertion1nstd209human GRCh38 chr2: 32,939,855-32,939,855 , GRCh37.p13 chr2: 33,164,922-33,164,922 LINC00486, LTBP1
    nsv5958052insertion1nstd209human GRCh38 chr2: 33,277,775-33,277,775 , GRCh37.p13 chr2: 33,502,842-33,502,842 LTBP1
    nsv5953534insertion1nstd209human GRCh38 chr2: 33,228,695-33,228,695 , GRCh37.p13 chr2: 33,453,762-33,453,762 LTBP1
    nsv5947769insertion1nstd209human GRCh38 chr2: 33,350,731-33,350,731 , GRCh37.p13 chr2: 33,575,798-33,575,798 LTBP1
    nsv5883466copy number variation1nstd209human GRCh38 chr2: 32,915,912-32,918,402 , GRCh37.p13 chr2: 33,140,979-33,143,469 LTBP1, LINC00486
    nsv5882675copy number variation1nstd209human GRCh38 chr2: 33,225,905-33,229,904 , GRCh37.p13 chr2: 33,450,972-33,454,971 LTBP1
    nsv5881141copy number variation1nstd209human GRCh38 chr2: 32,999,395-33,002,224 , GRCh37.p13 chr2: 33,224,462-33,227,291 LTBP1
    nsv5881031copy number variation1nstd209human GRCh38 chr2: 33,057,076-33,057,273 , GRCh37.p13 chr2: 33,282,143-33,282,340 LTBP1
    nsv5880096copy number variation1nstd209human GRCh38 chr2: 32,939,844-32,939,986 , GRCh37.p13 chr2: 33,164,911-33,165,053 LINC00486, LTBP1
    nsv5878300copy number variation1nstd209human GRCh38 chr2: 33,135,520-33,135,571 , GRCh37.p13 chr2: 33,360,587-33,360,638 LTBP1
    nsv5877609copy number variation1nstd209human GRCh38 chr2: 32,939,576-32,942,508 , GRCh37.p13 chr2: 33,164,643-33,167,575 LINC00486, LTBP1
    nsv5877043copy number variation1nstd209human GRCh38 chr2: 33,028,581-33,028,810 , GRCh37.p13 chr2: 33,253,648-33,253,877 LTBP1
    nsv5875197copy number variation1nstd209human GRCh38 chr2: 32,939,828-32,939,877 , GRCh37.p13 chr2: 33,164,895-33,164,944 LINC00486, LTBP1
    nsv5873889copy number variation1nstd209human GRCh38 chr2: 32,916,156-32,918,334 , GRCh37.p13 chr2: 33,141,223-33,143,401 LTBP1, LINC00486
    nsv5872617copy number variation1nstd209human GRCh38 chr2: 33,287,865-33,291,694 , GRCh37.p13 chr2: 33,512,932-33,516,761 LTBP1
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