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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074643inversion1nstd229human GRCh38 chr12: 123,471,880-125,706,144 , GRCh37.p13 chr12: 123,956,427-126,190,690 DHX37, RNU6-927P, 44 more genes
    nsv7074199inversion1nstd229human GRCh38 chr12: 123,186,434-132,825,682 , GRCh37.p13 chr12: 123,670,981-133,402,268 PIWIL1, FZD10-AS1, 187 more genes
    nsv6638030copy number variation1nstd102humanUncertain significance GRCh37 chr12: 125,346,689-126,135,525 , GRCh38.p12 chr12: 124,862,143-125,650,979 MIR5188, TRD-GTC2-10, 19 more genes
    nsv6581741inversion1nstd223human GRCh38 chr12: 123,471,879-125,706,143 , GRCh37.p13 chr12: 123,956,426-126,190,689 LOC105370042, TMEM132B, 44 more genes
    nsv6493055copy number variation1nstd223human GRCh38 chr12: 124,911,856-124,913,116 , GRCh37.p13 chr12: 125,396,402-125,397,583 UBC
    nsv6485432copy number variation1nstd223human GRCh38 chr12: 124,913,013-124,913,241 , GRCh37.p13 chr: NaN-NaN UBC
    nsv6290239copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 117,461,902-133,841,395 , GRCh38.p12 chr12: 117,024,097-133,264,809 ACADS, BCL7A, 356 more genes
    nsv6205369copy number variation1nstd214human GRCh38 chr12: 124,913,349-124,913,576 , GRCh37.p13 chr12: 125,397,895-125,398,122 UBC, MIR5188
    nsv6132143copy number variation1nstd213human GRCh37 chr12: 124,300,000-126,200,001 , GRCh38.p12 chr12: 123,815,453-125,715,455 UBC, DHX37, 29 more genes
    nsv6032976copy number variation1nstd212human GRCh38 chr12: 124,912,786-124,913,158 , GRCh37.p13 chr12: 125,397,332-125,397,583 UBC
    nsv6028660copy number variation1nstd212human GRCh38 chr12: 124,912,606-124,912,832 , GRCh37.p13 chr12: 125,397,152-125,397,378 UBC
    nsv6026476copy number variation1nstd212human GRCh38 chr12: 124,912,055-124,912,281 , GRCh37.p13 chr12: 125,396,601-125,396,827 UBC
    nsv5933483copy number variation1nstd209human GRCh38 chr12: 124,912,774-124,913,671 , GRCh37.p13 chr12: 125,397,320-125,398,217 UBC, MIR5188
    nsv5705785mobile element insertion1nstd211human GRCh38 chr12: 124,911,057-124,911,057 , GRCh37.p13 chr12: 125,395,603-125,395,603 UBC
    nsv5705682mobile element insertion1nstd211human GRCh38 chr12: 124,911,639-124,911,639 , GRCh37.p13 chr12: 125,396,185-125,396,185 UBC
    nsv5647532insertion1nstd207human GRCh38 chr12: 124,912,650-124,912,650 , GRCh37.p13 chr12: 125,397,196-125,397,196 UBC
    nsv5590923copy number variation1nstd207human GRCh38 chr12: 124,911,906-124,912,133 , GRCh37.p13 chr12: 125,396,452-125,396,679 UBC
    nsv5512662copy number variation1nstd206human GRCh38 chr12: 124,913,208-124,913,664 , GRCh37.p13 chr12: 125,397,584-125,398,210 UBC, MIR5188
    nsv5424616mobile element insertion1nstd206human GRCh38 chr12: 124,911,057-124,911,108 , GRCh37.p13 chr12: 125,395,603-125,395,654 UBC
    nsv5381782copy number variation1nstd102humanPathogenic GRCh37 chr12: 123,878,845-126,829,341 , GRCh38.p12 chr12: 123,394,298-126,344,795 DDX55, ZNF664, 55 more genes
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