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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5278867copy number variation1nstd204human GRCh38.p13 chr12: 114,635,601-114,733,300 , GRCh37.p13 chr12: 115,073,406-115,171,105 LOC105369999, TBX3, 1 more genes
    nsv4846182copy number variation1nstd200human GRCh37 chr12: 115,113,567-115,113,866 , GRCh38.p12 chr12: 114,675,762-114,676,061 TBX3
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 ACACB, ACADS, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 ACACB, ACADS, 1787 more genes
    nsv4754840inversion1nstd199human GRCh37 chr12: 104,382,539-125,801,164 , GRCh38.p12 chr12: 103,988,761-125,316,618 ACACB, ACADS, 452 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 RNA5SP368, LINC02555, 1787 more genes
    nsv3914194copy number variation1nstd102humanPathogenic NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807 GLYCAM1, LOC101927436, 2523 more genes
    nsv3913894copy number variation1nstd102humanPathogenic NCBI36 chr12: 113,190,591-132,287,975 , GRCh38 chr12: 114,268,403-133,201,316 , GRCh37 chr12: 114,706,208-133,777,902 ADGRD1, LOC105370012, 399 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 RAN, LOC100506606, 2524 more genes
    nsv3904719copy number variation1nstd102humanPathogenic GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532 LOC102724146, KRT75, 2513 more genes
    nsv3904242copy number variation1nstd102humanPathogenic GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309 NCKAP1L, MORF4L1P2, 2526 more genes
    nsv3903462copy number variation1nstd102humanPathogenic GRCh37 chr12: 112,963,559-116,095,198 , GRCh38.p12 chr12: 112,525,755-115,657,393 SDS, PLBD2, 47 more genes
    nsv3898489copy number variation1nstd102humanUncertain significance GRCh37 chr12: 114,948,986-115,167,687 , GRCh38.p12 chr12: 114,511,181-114,729,882 OSTF1P1, TBX3-AS1, 1 more genes
    nsv3897722copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059 LOC105369959, TMEM198B, 2524 more genes
    nsv3890891copy number variation1nstd102humanPathogenic GRCh37 chr12: 114,995,645-115,376,925 , GRCh38.p12 chr12: 114,557,840-114,939,120 TBX3, OSTF1P1, 3 more genes
    nsv3169098inversion1nstd158human GRCh37 chr12: 28,095,967-121,612,723 , GRCh38.p12 chr12: 27,943,034-121,174,920 ACACB, ACADS, 1642 more genes
    nsv3168340inversion1nstd158human GRCh37 chr12: 66,451,836-123,782,201 , GRCh38.p12 chr12: 66,058,056-123,297,654 ACACB, ACADS, 909 more genes
    nsv2772456copy number variation1nstd37humanPathogenic GRCh38.p12 chr12: 114,557,840-114,939,120 , GRCh37 chr12: 114,995,645-115,376,925 TBX3, OSTF1P1, 3 more genes
    nsv2771993copy number variation1nstd37humanPathogenic GRCh37 chr12: 112,963,559-116,095,198 , GRCh38.p12 chr12: 112,525,755-115,657,393 DTX1, TBX5, 47 more genes
    nsv2770609copy number variation3nstd37humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 , ABCD2, 2525 more genes
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