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Items: 1 to 20 of 353

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137696copy number variation1nstd232human GRCh37.p13 chr3: 32,163,059-32,163,168 , GRCh38.p12 chr3: 32,121,567-32,121,676 GPD1L
    nsv7044380inversion1nstd229human GRCh38 chr3: 32,075,032-32,211,739 , GRCh37.p13 chr3: 32,116,524-32,253,231 GPD1L, RPSAP11
    nsv6714800copy number variation1nstd229human GRCh38 chr3: 32,100,616-32,142,561 , GRCh37.p13 chr3: 32,142,108-32,184,053 GPD1L
    nsv6712313copy number variation1nstd229human GRCh38 chr3: 32,112,226-32,112,383 , GRCh37.p13 chr3: 32,153,718-32,153,875 GPD1L
    nsv6711166copy number variation1nstd229human GRCh38 chr3: 31,817,174-32,276,642 , GRCh37.p13 chr3: 31,858,666-32,318,134 RPSAP11, NIFKP7, 6 more genes
    nsv6710729copy number variation1nstd229human GRCh38 chr3: 32,119,979-32,129,356 , GRCh37.p13 chr3: 32,161,471-32,170,848 GPD1L
    nsv6710663copy number variation1nstd229human GRCh38 chr3: 32,137,249-32,140,660 , GRCh37.p13 chr3: 32,178,741-32,182,152 GPD1L
    nsv6710216copy number variation1nstd229human GRCh38 chr3: 32,112,743-32,112,870 , GRCh37.p13 chr3: 32,154,235-32,154,362 GPD1L
    nsv6702527copy number variation1nstd229human GRCh38 chr3: 32,163,001-32,165,200 , GRCh37.p13 chr3: 32,204,493-32,206,692 GPD1L
    nsv6700055copy number variation1nstd229human GRCh38 chr3: 32,140,657-32,140,686 , GRCh37.p13 chr3: 32,182,149-32,182,178 GPD1L
    nsv6699185copy number variation1nstd229human GRCh38 chr3: 31,838,889-32,352,737 , GRCh37.p13 chr3: 31,880,381-32,394,229 OSBPL10, KRT18P15, 6 more genes
    nsv6539882inversion1nstd223human GRCh38 chr3: 32,144,853-32,145,187 , GRCh37.p13 chr3: 32,186,345-32,186,679 GPD1L
    nsv6368302copy number variation1nstd223human GRCh38 chr3: 31,905,368-32,199,484 , GRCh37.p13 chr3: 31,946,860-32,240,976 GPD1L, OSBPL10, 4 more genes
    nsv6367352copy number variation1nstd223human GRCh38 chr3: 32,096,326-32,117,483 , GRCh37.p13 chr3: 32,137,818-32,158,975 GPD1L
    nsv6360709copy number variation1nstd223human GRCh38 chr3: 32,162,369-32,162,651 , GRCh37.p13 chr3: 32,203,861-32,204,143 GPD1L
    nsv6360563copy number variation1nstd223human GRCh38 chr3: 31,859,908-32,260,156 , GRCh37.p13 chr3: 31,901,400-32,301,648 ZNF860, KRT18P15, 6 more genes
    nsv6313891copy number variation1nstd102humanUncertain significance GRCh37 chr3: 31,859,973-33,127,072 , GRCh38.p12 chr3: 31,818,481-33,085,580 RPL30P4, RPL21P40, 22 more genes
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 LOC102724104, CRIP1P2, 291 more genes
    nsv6263570copy number variation1nstd214human GRCh38 chr3: 32,112,226-32,112,382 , GRCh37.p13 chr3: 32,153,718-32,153,874 GPD1L
    nsv6134843copy number variation1nstd213human GRCh37 chr3: 31,580,000-32,830,001 , GRCh38.p12 chr3: 31,538,508-32,788,509 GPD1L, CNOT10, 19 more genes
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