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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7046088inversion1nstd229human GRCh38 chr5: 72,326,212-72,326,302 , GRCh37.p13 chr5: 71,622,039-71,622,129 PTCD2
    nsv7039325inversion1nstd229human GRCh38 chr5: 72,333,301-72,333,332 , GRCh37.p13 chr5: 71,629,128-71,629,159 PTCD2
    nsv6777546copy number variation1nstd229human GRCh38 chr5: 72,317,501-72,323,900 , GRCh37.p13 chr5: 71,613,328-71,619,727 MRPS27, PTCD2
    nsv6777529copy number variation1nstd229human GRCh38 chr5: 72,324,027-72,330,071 , GRCh37.p13 chr5: 71,619,854-71,625,898 PTCD2
    nsv6772529copy number variation1nstd229human GRCh38 chr5: 72,366,735-72,399,263 , GRCh37.p13 chr5: 71,662,562-71,695,090 PTCD2, RPL10AP8
    nsv6763618copy number variation1nstd229human GRCh38 chr5: 66,450,908-74,585,645 , GRCh37.p13 chr5: 65,746,736-73,881,470 LOC107986372, LOC105379027, 146 more genes
    nsv6760091copy number variation1nstd229human GRCh38 chr5: 72,336,701-72,337,900 , GRCh37.p13 chr5: 71,632,528-71,633,727 PTCD2
    nsv6571416inversion1nstd223human GRCh38 chr5: 72,341,070-72,341,500 , GRCh37.p13 chr5: 71,636,897-71,637,327 PTCD2
    nsv6410266copy number variation1nstd223human GRCh38 chr5: 72,336,664-72,337,907 , GRCh37.p13 chr5: 71,632,491-71,633,734 PTCD2
    nsv6402735copy number variation1nstd223human GRCh38 chr5: 72,324,025-72,330,070 , GRCh37.p13 chr5: 71,619,852-71,625,897 PTCD2
    nsv6260488mobile element insertion1nstd215human GRCh38 chr5: 72,339,717-72,339,717 , GRCh37.p13 chr5: 71,635,544-71,635,544 PTCD2
    nsv6136131copy number variation1nstd213human GRCh37 chr5: 70,130,000-73,760,001 , GRCh38.p12 chr5: 70,834,173-74,464,176 , BTF3, 69 more genes
    nsv6135436copy number variation1nstd213human GRCh37 chr5: 70,260,000-91,630,001 , GRCh38.p12 chr5: 70,964,173-92,334,184 , ARSB, 300 more genes
    nsv6135435copy number variation1nstd213human GRCh37 chr5: 69,990,000-73,820,001 , GRCh38.p12 chr5: 70,694,173-74,524,176 , BTF3, 71 more genes
    nsv6135198copy number variation1nstd213human GRCh37 chr5: 70,130,000-76,140,001 , GRCh38.p12 chr5: 70,834,173-76,844,176 , BTF3, 117 more genes
    nsv6077590insertion1nstd212human GRCh38 chr5: 72,365,466-72,365,466 , GRCh37.p13 chr5: 71,661,293-71,661,293 PTCD2
    nsv6063349insertion1nstd212human GRCh38 chr5: 72,330,583-72,330,583 , GRCh37.p13 chr5: 71,626,410-71,626,410 PTCD2
    nsv5965617insertion1nstd209human GRCh38 chr5: 72,339,706-72,339,706 , GRCh37.p13 chr5: 71,635,533-71,635,533 PTCD2
    nsv5679865mobile element insertion2nstd211human GRCh38 chr5: 72,339,717-72,339,717 , GRCh37.p13 chr5: 71,635,544-71,635,544 PTCD2
    nsv5641872insertion1nstd207human GRCh38 chr5: 72,339,706-72,339,706 , GRCh37.p13 chr5: 71,635,533-71,635,533 PTCD2
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