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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
    nsv6137687copy number variation1nstd102humannot provided GRCh38 chr2: 36,472,472-36,866,823 , GRCh37.p13 chr2: 36,699,615-37,093,966 CRIM1, STRN, 4 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
    nsv5966663insertion1nstd209human GRCh38 chr2: 36,966,893-36,966,893 , GRCh37.p13 chr2: 37,194,036-37,194,036 STRN
    nsv5881324copy number variation1nstd209human GRCh38 chr2: 36,946,152-36,946,222 , GRCh37.p13 chr2: 37,173,295-37,173,365 STRN
    nsv5867719copy number variation1nstd209human GRCh38 chr2: 36,883,440-37,015,843 , GRCh37.p13 chr2: 37,110,583-37,242,986 HEATR5B, STRN
    nsv5833200copy number variation1nstd209human GRCh38 chr2: 36,919,026-36,968,152 , GRCh37.p13 chr2: 37,146,169-37,195,295 STRN
    nsv5833198copy number variation1nstd209human GRCh38 chr2: 36,889,654-36,892,253 , GRCh37.p13 chr2: 37,116,797-37,119,396 STRN
    nsv5833197copy number variation1nstd209human GRCh38 chr2: 36,882,129-36,886,328 , GRCh37.p13 chr2: 37,109,272-37,113,471 STRN
    nsv5832974copy number variation1nstd209human GRCh38 chr2: 36,883,447-36,914,888 , GRCh37.p13 chr2: 37,110,590-37,142,031 STRN
    nsv5832634copy number variation1nstd209human GRCh38 chr2: 36,964,639-36,974,365 , GRCh37.p13 chr2: 37,191,782-37,201,508 STRN
    nsv5620976insertion1nstd207human GRCh38 chr2: 36,923,501-36,923,501 , GRCh37.p13 chr2: 37,150,644-37,150,644 STRN
    nsv5607858insertion2nstd207human GRCh38 chr2: 36,966,898-36,966,898 , GRCh37.p13 chr2: 37,194,041-37,194,041 STRN
    nsv5575519copy number variation1nstd207human GRCh38 chr2: 36,919,498-36,919,915 , GRCh37.p13 chr2: 37,146,641-37,147,058 STRN
    nsv5574558copy number variation1nstd207human GRCh38 chr2: 36,931,081-36,931,147 , GRCh37.p13 chr2: 37,158,224-37,158,290 STRN
    nsv5443954copy number variation1nstd206human GRCh38 chr2: 36,966,813-36,966,874 , GRCh37.p13 chr2: 37,193,956-37,194,017 STRN
    nsv5438601copy number variation1nstd206human GRCh38 chr2: 36,897,517-36,897,601 , GRCh37.p13 chr2: 37,124,660-37,124,744 STRN
    nsv5436539copy number variation1nstd206human GRCh38 chr2: 36,912,151-36,912,345 , GRCh37.p13 chr2: 37,139,294-37,139,488 STRN
    nsv5359117translocation1nstd200human GRCh38 chr2: 36,925,763-36,925,763 , GRCh38 chr2: 36,925,661-36,925,661 , GRCh37.p13 chr2: 37,152,906-37,152,906 , GRCh37.p13 chr2: 37,152,804-37,152,804 STRN
    nsv5198195mobile element insertion1nstd203human GRCh38 chr2: 36,944,449-36,944,461 , GRCh37.p13 chr2: 37,171,592-37,171,604 STRN
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