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Items: 1 to 20 of 110

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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
    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
    nsv5933483copy number variation1nstd209human GRCh38 chr12: 124,912,774-124,913,671 , GRCh37.p13 chr12: 125,397,320-125,398,217 UBC, MIR5188
    nsv5512662copy number variation1nstd206human GRCh38 chr12: 124,913,208-124,913,664 , GRCh37.p13 chr12: 125,397,584-125,398,210 UBC, MIR5188
    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
    nsv4831190copy number variation1nstd200human GRCh37 chr12: 125,397,251-125,398,255 , GRCh38.p12 chr12: 124,912,705-124,913,709 MIR5188, UBC
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4754840inversion1nstd199human GRCh37 chr12: 104,382,539-125,801,164 , GRCh38.p12 chr12: 103,988,761-125,316,618 , ACACB, 452 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4455692copy number variation1nstd102humanPathogenic GRCh37 chr12: 122,169,403-129,084,163 , GRCh38.p12 chr12: 121,731,497-128,599,618 LOC107987176, LRRC43, 147 more genes
    nsv4231212copy number variation1nstd166human GRCh37.p13 chr12: 125,397,000-125,402,200 , GRCh38.p12 chr12: 124,912,454-124,917,654 UBC, MIR5188
    nsv3924220copy number variation1nstd102humanPathogenic GRCh38 chr12: 115,131,583-133,166,920 , NCBI36 chr12: 114,053,771-132,253,579 , GRCh37 chr12: 115,569,388-133,743,506 LOC105370080, LINC02985, 376 more genes
    nsv3923612copy number variation1nstd102humanPathogenic GRCh38 chr12: 120,718,786-127,500,215 , GRCh37 chr12: 121,156,589-127,984,760 , NCBI36 chr12: 119,640,972-126,550,713 NCOR2, LOC105378258, 161 more genes
    nsv3923347copy number variation1nstd102humanPathogenic NCBI36 chr12: 119,619,858-132,289,149 , GRCh37 chr12: 121,135,475-133,779,076 , GRCh38 chr12: 120,697,672-133,202,490 LOC105370044, RNU6-1017P, 273 more genes
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