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Items: 1 to 20 of 98

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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
    nsv7037485copy number variation1nstd229human GRCh38 chr20: 60,306,756-60,317,439 , GRCh37.p13 chr20: 58,881,814-58,892,497 MIR646, MIR646HG
    nsv7037078copy number variation1nstd229human GRCh38 chr20: 54,988,450-63,850,628 , GRCh37.p13 chr20: 53,604,989-62,481,981 , RPL39P, 209 more genes
    nsv7030948copy number variation1nstd229human GRCh38 chr20: 60,307,142-60,307,268 , GRCh37.p13 chr20: 58,882,200-58,882,326 MIR646HG, MIR646
    nsv7021100copy number variation1nstd229human GRCh38 chr20: 59,995,939-60,524,337 , GRCh37.p13 chr20: 58,570,994-59,099,395 LINC02910, MIR4533, 8 more genes
    nsv6553698copy number variation1nstd223human GRCh38 chr20: 60,307,142-60,307,268 , GRCh37.p13 chr20: 58,882,200-58,882,326 MIR646, MIR646HG
    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
    nsv6227167copy number variation1nstd214human GRCh38 chr20: 60,307,142-60,307,267 , GRCh37.p13 chr20: 58,882,200-58,882,325 MIR646, MIR646HG
    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
    nsv6134045copy number variation1nstd213human GRCh37 chr20: 58,760,000-60,230,001 , GRCh38.p12 chr20: 60,184,942-61,654,945 LINC01718, LOC105372698, 12 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
    nsv6052227copy number variation1nstd212human GRCh38 chr20: 60,307,142-60,307,268 , GRCh37.p13 chr20: 58,882,200-58,882,326 MIR646, MIR646HG
    nsv5966731copy number variation1nstd209human GRCh38 chr20: 60,307,142-60,307,267 , GRCh37.p13 chr20: 58,882,200-58,882,325 MIR646, MIR646HG
    nsv5603421copy number variation1nstd207human GRCh38 chr20: 60,307,142-60,307,267 , GRCh37.p13 chr20: 58,882,200-58,882,325 MIR646, MIR646HG
    nsv5525967copy number variation1nstd206human GRCh38 chr20: 60,307,142-60,307,268 , GRCh37.p13 chr20: 58,882,200-58,882,326 MIR646, MIR646HG
    nsv5324839copy number variation1nstd204human GRCh37.p13 chr20: 58,882,200-58,882,326 , GRCh38.p13 chr20: 60,307,142-60,307,268 MIR646, MIR646HG
    nsv5025771copy number variation1nstd200human GRCh38 chr20: 60,155,509-60,990,304 , GRCh37.p13 chr20: 58,730,565-59,565,360 MIR646, MIR4533, 8 more genes
    nsv5013403copy number variation1nstd200human GRCh38 chr20: 60,307,142-60,307,268 , GRCh37.p13 chr20: 58,882,200-58,882,326 MIR646HG, MIR646
    nsv5013402copy number variation1nstd200human GRCh38 chr20: 60,305,923-60,307,532 , GRCh37.p13 chr20: 58,880,981-58,882,590 MIR646, MIR646HG
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