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Items: 1 to 20 of 145

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148267copy number variation1nstd102humanPathogenic GRCh38 chr20: 87,153-23,635,465 , GRCh37.p13 chr20: 67,794-23,616,102 KRT18P3, RSPO4, 413 more genes
    nsv7072011inversion1nstd229human GRCh38 chr20: 19,125,473-21,611,699 , GRCh37.p13 chr20: 19,106,117-21,592,337 SLC24A3, GSTM3P1, 35 more genes
    nsv7065399inversion1nstd229human GRCh38 chr20: 13,871,578-20,212,622 , GRCh37.p13 chr20: 13,852,224-20,193,266 SLC24A3, LOC107985418, 92 more genes
    nsv7037623copy number variation1nstd229human GRCh38 chr20: 19,966,651-20,053,714 , GRCh37.p13 chr20: 19,947,295-20,034,358 CRNKL1, CFAP61, 2 more genes
    nsv6528967copy number variation1nstd223human GRCh38 chr20: 20,030,949-20,031,565 , GRCh37.p13 chr20: 20,011,593-20,012,209 NAA20
    nsv6516420copy number variation1nstd223human GRCh38 chr20: 20,032,015-20,032,459 , GRCh37.p13 chr20: 20,012,659-20,013,103 NAA20, CRNKL1
    nsv6314164copy number variation1nstd102humanPathogenic GRCh37 chr20: 19,292,925-22,187,397 , GRCh38.p12 chr20: 19,312,281-22,206,759 SLC25A6P1, RPL41P1, 37 more genes
    nsv6291578copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 18,665,879-33,903,216 , GRCh38.p12 chr20: 18,685,235-35,315,413 AHCY, ASIP, 330 more genes
    nsv6134275copy number variation1nstd213human GRCh37 chr20: 19,430,000-23,860,001 , GRCh38.p12 chr20: 19,449,356-23,879,364 CST1, CST4, 87 more genes
    nsv6134268copy number variation1nstd213human GRCh37 chr20: 13,380,000-22,450,001 , GRCh38.p12 chr20: 13,399,353-22,469,363 BFSP1, INSM1, 134 more genes
    nsv6133905copy number variation1nstd213human GRCh37 chr20: 20,010,000-20,220,001 , GRCh38.p12 chr20: 20,029,356-20,239,357 CFAP61, NAA20, 2 more genes
    nsv5950938copy number variation1nstd209human GRCh38 chr20: 20,032,015-20,032,456 , GRCh37.p13 chr20: 20,012,659-20,013,100 NAA20, CRNKL1
    nsv5874016copy number variation1nstd209human GRCh38 chr20: 20,025,628-20,026,627 , GRCh37.p13 chr20: 20,006,272-20,007,271 NAA20
    nsv5529933copy number variation1nstd206human GRCh38 chr20: 20,023,055-20,023,632 , GRCh37.p13 chr20: 20,003,699-20,004,276 , NAA20
    nsv5515004copy number variation1nstd206human GRCh38 chr20: 20,032,015-20,032,459 , GRCh37.p13 chr20: 20,012,659-20,013,103 CRNKL1, NAA20
    nsv5389730copy number variation3nstd186human GRCh37 chr20: 20,012,659-20,013,103 , GRCh38.p12 chr20: 20,032,015-20,032,459 NAA20, CRNKL1
    nsv5320460copy number variation1nstd204human GRCh37.p13 chr20: 20,012,654-20,013,112 , GRCh38.p13 chr20: 20,032,010-20,032,468 CRNKL1, NAA20
    nsv5021635copy number variation1nstd200human GRCh38 chr20: 20,032,015-20,032,459 , GRCh37.p13 chr20: 20,012,659-20,013,103 CRNKL1, NAA20
    nsv4862275copy number variation1nstd200human GRCh37 chr20: 20,012,659-20,013,103 , GRCh38.p12 chr20: 20,032,015-20,032,459 NAA20, CRNKL1
    nsv4729757copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 19,750,804-30,479,077 , GRCh38.p12 chr20: 19,770,160-31,891,274 BCL2L1, CD24P3, 222 more genes
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