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Items: 1 to 20 of 1105

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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
    nsv6119514copy number variation1nstd186human GRCh37 chr2: 40,480,201-40,480,276 , GRCh38.p12 chr2: 40,253,061-40,253,136 SLC8A1-AS1, SLC8A1
    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
    nsv5971119inversion1nstd209human GRCh38 chr2: 40,252,807-40,252,911 , GRCh37.p13 chr2: 40,479,947-40,480,051 SLC8A1, SLC8A1-AS1
    nsv5953741insertion1nstd209human GRCh38 chr2: 40,054,975-40,054,975 , GRCh37.p13 chr2: 40,282,115-40,282,115 SLC8A1-AS1
    nsv5882910copy number variation1nstd209human GRCh38 chr2: 40,219,806-40,219,932 , GRCh37.p13 chr2: 40,446,946-40,447,072 SLC8A1-AS1, SLC8A1
    nsv5881082copy number variation1nstd209human GRCh38 chr2: 40,022,212-40,028,561 , GRCh37.p13 chr2: 40,249,352-40,255,701 SLC8A1-AS1
    nsv5877266copy number variation1nstd209human GRCh38 chr2: 40,251,973-40,252,037 , GRCh37.p13 chr2: 40,479,113-40,479,177 SLC8A1-AS1, SLC8A1
    nsv5877235copy number variation1nstd209human GRCh38 chr2: 40,255,678-40,255,728 , GRCh37.p13 chr2: 40,482,818-40,482,868 SLC8A1, SLC8A1-AS1
    nsv5875118copy number variation1nstd209human GRCh38 chr2: 40,072,682-40,097,932 , GRCh37.p13 chr2: 40,299,822-40,325,072 SLC8A1, SLC8A1-AS1
    nsv5874910copy number variation1nstd209human GRCh38 chr2: 39,914,966-39,997,877 , GRCh37.p13 chr2: 40,142,106-40,225,017 SLC8A1-AS1, LOC100419512
    nsv5873926copy number variation1nstd209human GRCh38 chr2: 40,050,872-40,054,253 , GRCh37.p13 chr2: 40,278,012-40,281,393 SLC8A1-AS1
    nsv5873384copy number variation1nstd209human GRCh38 chr2: 40,005,554-40,015,668 , GRCh37.p13 chr2: 40,232,694-40,242,808 SLC8A1-AS1
    nsv5872658copy number variation1nstd209human GRCh38 chr2: 40,197,815-40,197,864 , GRCh37.p13 chr2: 40,424,955-40,425,004 SLC8A1, SLC8A1-AS1
    nsv5868185copy number variation1nstd209human GRCh38 chr2: 40,064,605-40,064,740 , GRCh37.p13 chr2: 40,291,745-40,291,880 SLC8A1-AS1
    nsv5868079copy number variation1nstd209human GRCh38 chr2: 40,254,452-40,254,507 , GRCh37.p13 chr2: 40,481,592-40,481,647 SLC8A1, SLC8A1-AS1
    nsv5833234copy number variation1nstd209human GRCh38 chr2: 40,072,713-40,086,160 , GRCh37.p13 chr2: 40,299,853-40,313,300 SLC8A1-AS1
    nsv5833233copy number variation1nstd209human GRCh38 chr2: 40,005,489-40,015,489 , GRCh37.p13 chr2: 40,232,629-40,242,629 SLC8A1-AS1
    nsv5833232copy number variation1nstd209human GRCh38 chr2: 39,962,058-39,963,644 , GRCh37.p13 chr2: 40,189,198-40,190,784 SLC8A1-AS1
    nsv5833220copy number variation1nstd209human GRCh38 chr2: 40,087,761-40,098,020 , GRCh37.p13 chr2: 40,314,901-40,325,160 SLC8A1, SLC8A1-AS1
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