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Items: 1 to 20 of 78

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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
    nsv7073102inversion1nstd229human GRCh38 chr20: 58,529,050-58,860,387 , GRCh37.p13 chr20: 57,104,106-57,435,442 NPEPL1, MIR298, 10 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
    nsv6537321copy number variation1nstd223human GRCh38 chr20: 58,450,646-58,832,496 , GRCh37.p13 chr20: 57,025,702-57,407,551 STX16-NPEPL1, LOC107985410, 11 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
    nsv6314094copy number variation1nstd102humanPathogenic GRCh37 chr20: 55,292,205-57,866,365 , GRCh38.p12 chr20: 56,717,149-59,291,310 PCK1, MIR296, 58 more genes
    nsv6311086copy number variation1nstd102humanUncertain significance GRCh37 chr20: 54,823,900-57,899,514 , GRCh38.p12 chr20: 56,248,844-59,324,459 CTSZ, SPO11, 75 more genes
    nsv6134308copy number variation1nstd213human GRCh37 chr20: 55,660,000-60,880,001 , GRCh38.p12 chr20: 57,084,944-62,304,945 TAF4, OSBPL2, 97 more genes
    nsv6134174copy number variation1nstd213human GRCh37 chr20: 57,120,000-57,640,001 , GRCh38.p12 chr20: 58,544,944-59,064,946 SLMO2-ATP5E, LOC105372695, 19 more genes
    nsv6134040copy number variation1nstd213human GRCh37 chr20: 51,820,000-60,870,001 , GRCh38.p12 chr20: 53,203,461-62,294,945 MC3R, PPP1R3D, 142 more genes
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv4676332copy number variation1nstd102humanPathogenic GRCh37 chr20: 55,743,522-62,032,989 , GRCh38.p12 chr20: 57,168,466-63,401,636 BMP7, MIR298, 153 more genes
    nsv4676181copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,788,101-62,762,405 , GRCh38.p12 chr20: 58,213,045-64,131,052 LOC105372697, MIR647, 174 more genes
    nsv4506799mobile element insertion1nstd166human GRCh37.p13 chr20: 57,348,592-57,348,592 , GRCh38.p12 chr20: 58,773,536-58,773,536 LOC105372695
    nsv4357849copy number variation1nstd102humanPathogenic GRCh37 chr20: 54,143,747-62,194,881 , GRCh38.p12 chr20: 55,568,689-63,563,528 RBM38, LAMA5, 192 more genes
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
    nsv3916118copy number variation1nstd102humanUncertain significance GRCh37 chr20: 57,205,529-57,456,724 , NCBI36 chr20: 56,638,935-56,890,119 , GRCh38 chr20: 58,630,473-58,881,669 MIR296, PIEZO1P2, 10 more genes
    nsv3915005copy number variation1nstd102humanPathogenic NCBI36 chr20: 42,849,759-62,379,118 , GRCh37 chr20: 43,416,345-62,908,674 , GRCh38 chr20: 44,787,704-64,277,321 FTLP1, RNA5SP487, 472 more genes
    nsv3912982copy number variation1nstd102humanLikely pathogenic NCBI36 chr20: 53,639,062-58,949,658 , GRCh37 chr20: 54,220,678-59,516,263 , GRCh38 chr20: 55,630,597-60,941,207 ATP5F1E, BMP7, 103 more genes
    nsv3911673copy number variation1nstd102humanPathogenic GRCh37 chr20: 54,773,088-62,908,674 , NCBI36 chr20: 54,206,495-62,379,118 , GRCh38 chr20: 56,198,032-64,277,321 LOC105372709, NPBWR2, 226 more genes
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