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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147571copy number variation1nstd232human GRCh37.p13 chr21: 47,322,167-47,322,226 , GRCh38.p12 chr21: 45,902,253-45,902,312 PCBP3
    nsv7144482copy number variation1nstd232human GRCh37.p13 chr21: 47,318,200-47,318,277 , GRCh38.p12 chr21: 45,898,286-45,898,363 PCBP3
    nsv7144125insertion1nstd232human GRCh37.p13 chr21: 47,159,256-47,159,256 , GRCh38.p12 chr21: 45,739,342-45,739,342 PCBP3
    nsv7143916copy number variation1nstd232human GRCh37.p13 chr21: 47,306,514-47,306,565 , GRCh38.p12 chr21: 45,886,600-45,886,651 PCBP3
    nsv7143641copy number variation1nstd232human GRCh37.p13 chr21: 47,234,350-47,234,406 , GRCh38.p12 chr21: 45,814,436-45,814,492 PCBP3
    nsv7143329copy number variation1nstd232human GRCh37.p13 chr21: 47,329,682-47,329,766 , GRCh38.p12 chr21: 45,909,768-45,909,852 PCBP3
    nsv7141425copy number variation1nstd232human GRCh37.p13 chr21: 47,234,356-47,234,405 , GRCh38.p12 chr21: 45,814,442-45,814,491 PCBP3
    nsv7141154insertion1nstd232human GRCh37.p13 chr21: 47,159,245-47,159,245 , GRCh38.p12 chr21: 45,739,331-45,739,331 PCBP3
    nsv7140637copy number variation1nstd232human GRCh37.p13 chr21: 47,344,760-47,344,884 , GRCh38.p12 chr21: 45,924,846-45,924,970 PCBP3
    nsv7140213insertion1nstd232human GRCh37.p13 chr21: 47,313,491-47,313,491 , GRCh38.p12 chr21: 45,893,577-45,893,577 PCBP3
    nsv7139351copy number variation1nstd232human GRCh37.p13 chr21: 47,318,568-47,318,699 , GRCh38.p12 chr21: 45,898,654-45,898,785 PCBP3
    nsv7138498insertion1nstd232human GRCh37.p13 chr21: 47,236,024-47,236,024 , GRCh38.p12 chr21: 45,816,110-45,816,110 PCBP3
    nsv7137944insertion1nstd232human GRCh37.p13 chr21: 47,316,789-47,316,789 , GRCh38.p12 chr21: 45,896,875-45,896,875 PCBP3
    nsv7096096copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr21: 43,160,998-47,754,702 , GRCh38.p12 chr21: 41,740,838-46,334,788 TSPEAR, LINC01424, 158 more genes
    nsv7076114inversion1nstd229human GRCh38 chr21: 45,722,281-45,939,276 , GRCh37.p13 chr21: 47,142,195-47,359,190 PCBP3, PCBP3-AS1
    nsv7076050inversion1nstd229human GRCh38 chr21: 45,605,764-46,186,956 , GRCh37.p13 chr21: 47,025,678-47,606,870 SPATC1L, PCBP3, 11 more genes
    nsv7075696inversion1nstd229human GRCh38 chr21: 45,887,626-45,945,781 , GRCh37.p13 chr21: 47,307,540-47,365,695 PCBP3
    nsv7067822inversion1nstd229human GRCh38 chr21: 45,504,401-46,041,263 , GRCh37.p13 chr21: 46,924,315-47,461,177 COL6A1, COL18A1, 8 more genes
    nsv7066570inversion1nstd229human GRCh38 chr21: 45,824,496-45,828,865 , GRCh37.p13 chr21: 47,244,410-47,248,779 PCBP3, PCBP3-AS1
    nsv7037830copy number variation1nstd229human GRCh38 chr21: 45,818,767-45,821,153 , GRCh37.p13 chr21: 47,238,681-47,241,067 PCBP3
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