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Items: 1 to 20 of 311

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148186copy number variation1nstd102humanUncertain significance GRCh37 chr20: 52,773,668-62,965,020 , GRCh38.p12 chr20: 54,157,129-64,333,667 LOC105372717, CTCFL, 245 more genes
    nsv7148178copy number variation1nstd102humanPathogenic GRCh38 chr20: 62,632,017-63,794,804 , GRCh37.p13 chr20: 61,267,734-62,426,157 GID8, TCFL5, 60 more genes
    nsv7137309insertion1nstd232human GRCh37.p13 chr20: 61,538,710-61,538,710 , GRCh38.p12 chr20: 62,907,358-62,907,358 DIDO1
    nsv7096264copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,680,869 , GRCh38.p12 chr20: 62,256,185-64,049,516 RPS21, MIR1-1HG, 102 more genes
    nsv7095910copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,471,874-62,078,210 , GRCh38.p12 chr20: 62,840,522-63,446,857 LINC01749, HAR1A, 32 more genes
    nsv7075234inversion1nstd229human GRCh38 chr20: 62,886,537-63,022,704 , GRCh37.p13 chr20: 61,517,889-61,654,056 LINC01749, GID8, 3 more genes
    nsv7071843inversion1nstd229human GRCh38 chr20: 62,912,832-62,944,154 , GRCh37.p13 chr20: 61,544,184-61,575,506 DIDO1, GID8
    nsv7064962inversion1nstd229human GRCh38 chr20: 62,710,955-62,963,614 , GRCh37.p13 chr20: 61,342,307-61,594,966 , GID8, 14 more genes
    nsv7037078copy number variation1nstd229human GRCh38 chr20: 54,988,450-63,850,628 , GRCh37.p13 chr20: 53,604,989-62,481,981 , RPL39P, 209 more genes
    nsv7030829copy number variation1nstd229human GRCh38 chr20: 62,902,098-62,902,297 , GRCh37.p13 chr20: 61,533,450-61,533,649 DIDO1
    nsv7023863copy number variation1nstd229human GRCh38 chr20: 62,879,328-62,879,359 , GRCh37.p13 chr20: 61,510,680-61,510,711 DIDO1
    nsv7020490copy number variation1nstd229human GRCh38 chr20: 62,767,801-62,877,700 , GRCh37.p13 chr20: 61,399,153-61,509,052 , DIDO1, 10 more genes
    nsv6637836copy number variation1nstd102humanUncertain significance GRCh37 chr20: 60,621,074-62,915,555 , GRCh38.p12 chr20: 62,046,018-64,284,202 SLC17A9, MIR3195, 120 more genes
    nsv6626803copy number variation1nstd224human GRCh37 chr20: 61,502,405-61,513,430 , GRCh38.p12 chr20: 62,871,053-62,882,078 ARF4P2, DIDO1, 2 more genes
    nsv6598511inversion1nstd223human GRCh38 chr20: 62,882,985-62,883,696 , GRCh37.p13 chr20: 61,514,337-61,515,048 DIDO1, SNORA117
    nsv6543382copy number variation1nstd223human GRCh38 chr20: 62,932,244-62,933,941 , GRCh37.p13 chr20: 61,563,596-61,565,293 DIDO1
    nsv6540637copy number variation1nstd223human GRCh38 chr20: 62,937,201-62,938,800 , GRCh37.p13 chr20: 61,568,553-61,570,152 DIDO1, GID8
    nsv6538338copy number variation1nstd223human GRCh38 chr20: 62,908,105-62,940,494 , GRCh37.p13 chr20: 61,539,457-61,571,846 GID8, DIDO1
    nsv6315308copy number variation1nstd102humanUncertain significance GRCh38 chr20: 61,800,345-63,644,611 , GRCh37.p13 chr20: 60,375,401-62,275,964 STMN3, RPS21, 86 more genes
    nsv6314208copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,835,739-62,915,555 , GRCh38.p12 chr20: 58,260,683-64,284,202 LOC105372698, LOC105372695, 176 more genes
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