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Items: 1 to 20 of 171

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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
    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
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 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
    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
    nsv3971839copy number variation1nstd102humannot provided GRCh38 chr12: 1-9,000,000 , GRCh37.p13 chr12: 282,465-9,152,596 RNU4ATAC16P, RNU6-174P, 257 more genes
    nsv3924262copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,835,837 , GRCh38 chr12: 64,620-34,682,902 , NCBI36 chr12: 44,047-34,727,104 ENO2, SLC6A13, 684 more genes
    nsv3922302copy number variation1nstd102humanPathogenic NCBI36 chr12: 17,360-6,924,620 , GRCh37 chr12: 147,099-7,054,359 , GRCh38 chr12: 45,740-6,945,196 HSPA8P5, LOC105369594, 172 more genes
    nsv3922178copy number variation1nstd102humanPathogenic GRCh37 chr12: 2,980,907-15,140,282 , NCBI36 chr12: 2,851,168-15,031,549 , GRCh38 chr12: 2,871,741-14,987,348 H2AJ, GPR162, 378 more genes
    nsv3919557copy number variation1nstd102humanPathogenic NCBI36 chr12: 59,934-11,147,715 , GRCh37.p13 chr12: 189,673-11,256,448 , GRCh38.p12 chr12: 80,507-11,103,849 ING4, LINC02827, 350 more genes
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