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Items: 1 to 20 of 352

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073526inversion1nstd229human GRCh38 chr18: 53,651,514-59,638,513 , GRCh37.p13 chr18: 51,177,884-57,305,745 MBD2, LOC105372145, 78 more genes
    nsv7064376inversion1nstd229human GRCh38 chr18: 54,203,129-54,203,187 , GRCh37.p13 chr18: 51,729,499-51,729,557 MBD2
    nsv7013654copy number variation1nstd229human GRCh38 chr18: 54,166,614-54,166,929 , GRCh37.p13 chr18: 51,692,984-51,693,299 MBD2
    nsv7007649copy number variation1nstd229human GRCh38 chr18: 54,169,317-54,169,441 , GRCh37.p13 chr18: 51,695,687-51,695,811 MBD2
    nsv7003631copy number variation1nstd229human GRCh38 chr18: 53,358,736-54,382,002 , GRCh37.p13 chr18: 50,885,106-51,908,372 POLI, MBD2, 7 more genes
    nsv7001908copy number variation1nstd229human GRCh38 chr18: 54,170,913-54,173,170 , GRCh37.p13 chr18: 51,697,283-51,699,540 MBD2
    nsv6637851copy number variation1nstd102humanUncertain significance GRCh37 chr18: 51,223,984-53,001,044 , GRCh38.p12 chr18: 53,697,614-55,333,813 MBD2, LINC03035, 15 more genes
    nsv6637509copy number variation1nstd102humanUncertain significance GRCh37 chr18: 49,666,138-51,804,494 , GRCh38.p12 chr18: 52,139,768-54,278,124 MIR4528, MBD2, 8 more genes
    nsv6581925inversion1nstd223human GRCh38 chr18: 54,156,680-54,157,409 , GRCh37.p13 chr18: 51,683,050-51,683,779 MBD2
    nsv6531879copy number variation1nstd223human GRCh38 chr18: 54,194,326-54,194,735 , GRCh37.p13 chr18: 51,720,696-51,721,105 MBD2
    nsv6522779copy number variation1nstd223human GRCh38 chr18: 54,209,209-54,221,350 , GRCh37.p13 chr18: 51,735,579-51,747,720 MBD2, SNORA37
    nsv6519884copy number variation1nstd223human GRCh38 chr18: 54,174,401-54,177,200 , GRCh37.p13 chr18: 51,700,771-51,703,570 MBD2
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
    nsv6314029copy number variation1nstd102humanPathogenic GRCh37 chr18: 50,707,829-54,924,248 , GRCh38.p12 chr18: 53,181,459-57,257,017 RNA5SP459, POLI, 42 more genes
    nsv6133333copy number variation1nstd213human GRCh37 chr18: 27,400,000-52,060,001 , GRCh38.p12 chr18: 29,820,035-54,532,766 ATP5F1A, DCC, 259 more genes
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv6111684insertion1nstd212human GRCh38 chr18: 54,200,195-54,200,195 , GRCh37.p13 chr18: 51,726,565-51,726,565 MBD2
    nsv6106219insertion1nstd212human GRCh38 chr18: 54,172,066-54,172,066 , GRCh37.p13 chr18: 51,698,436-51,698,436 MBD2
    nsv6035121copy number variation1nstd212human GRCh38 chr18: 54,156,432-54,156,520 , GRCh37.p13 chr18: 51,682,802-51,682,890 MBD2
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