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Items: 1 to 20 of 131

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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
    nsv5279702copy number variation1nstd204human GRCh38.p13 chr12: 6,507,601-6,909,400 , GRCh37.p13 chr12: 6,616,767-6,907,580 ING4, LPAR5, 30 more genes
    nsv5261405copy number variation1nstd204human GRCh38.p13 chr12: 6,720,401-6,891,700 , GRCh37.p13 chr12|NW_003871083.2: 1-93,284 , GRCh37.p13 chr12: 6,907,581-7,000,864 DSTNP2, RPL13P5, 14 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
    nsv4456206copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,872,484-7,009,333 , GRCh38.p12 chr12: 6,763,318-6,900,169 LOC105369632, SPSB2, 12 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
    nsv4416128copy number variation1nstd174human GRCh37 chr12: 6,791,348-6,888,380 , GRCh38.p12 chr12: 6,682,182-6,779,214 LAG3, PTMS, 5 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
    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
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