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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112763copy number variation1nstd102humanPathogenic GRCh37 chr12: 189,145-7,730,395 , GRCh38.p12 chr12: 79,979-7,577,799 GALNT8, LINC02371, 197 more genes
    nsv5968724inversion1nstd209human GRCh38 chr12: 6,473,720-6,709,618 , GRCh37.p13 chr12: 6,582,886-6,818,784 CHD4, GAPDH, 15 more genes
    nsv5564211copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,438,478-7,362,819 , GRCh38.p12 chr12: 6,329,312-7,210,223 GPR162, SCARNA11, 68 more genes
    nsv5562873sequence alteration1nstd206human GRCh38 chr12: 6,427,941-6,515,260 , GRCh37.p13 chr12: 6,537,107-6,624,426 CD27, VAMP1, 7 more genes
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5274829copy number variation1nstd204human GRCh38.p13 chr12: 6,429,601-6,613,800 , GRCh37.p13 chr12: 6,538,767-6,722,966 MRPL51, CHD4, 14 more genes
    nsv4974266copy number variation1nstd200human GRCh38 chr12: 6,158,793-6,527,112 , GRCh37.p13 chr12: 6,267,959-6,636,278 , TAPBPL, 22 more genes
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4682489copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,438,458-7,362,839 , GRCh38.p12 chr12: 6,329,292-7,210,243 MIR200CHG, MIR200C, 68 more genes
    nsv4675526copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,523,329-6,606,738 , GRCh38.p12 chr12: 6,414,163-6,497,572 VAMP1, NCAPD2, 6 more genes
    nsv4675304copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,528,194-6,606,738 , GRCh38.p12 chr12: 6,419,028-6,497,572 PKP2P1, SRP14P1, 6 more genes
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
    nsv4456650copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,070,459-6,737,675 , GRCh38.p12 chr12: 5,961,293-6,628,509 NOP2, PKP2P1, 32 more genes
    nsv4455658copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-8,393,815 , GRCh38.p12 chr12: 64,620-8,241,219 PLEKHG6, MIR141, 226 more genes
    nsv4455458copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,496,628 , GRCh38.p12 chr12: 64,620-34,343,693 EMP1, PLBD1-AS1, 684 more genes
    nsv4350818copy number variation1nstd102humanPathogenic GRCh37 chr12: 189,216-15,001,420 , GRCh38.p12 chr12: 80,050-14,848,486 LOC107984495, KLRC1, 432 more genes
    nsv4349513copy number variation1nstd102humanPathogenic GRCh37 chr12: 189,216-8,185,497 , GRCh38.p12 chr12: 80,050-8,032,901 LOC105369617, LRTM2, 214 more genes
    nsv4348793copy number variation1nstd102humanPathogenic GRCh37 chr12: 237,588-8,278,292 , GRCh38.p12 chr12: 128,422-8,125,696 RN7SL69P, GAPDH-DT, 216 more genes
    nsv4324171inversion1nstd166human GRCh37.p13 chr12: 6,338,819-22,046,498 , GRCh38.p12 chr12: 6,229,653-21,893,564 , APOBEC1, 414 more genes
    nsv4205161copy number variation1nstd166human GRCh37.p13 chr12: 6,464,359-6,646,359 , GRCh38.p12 chr12: 6,355,193-6,537,193 CD27-AS1, LOC107984500, 15 more genes
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