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Items: 1 to 20 of 136

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5381757copy number variation1nstd102humanPathogenic GRCh37 chr14: 33,608,925-44,570,367 , GRCh38.p12 chr14: 33,139,719-44,101,164 RPLP0P3, KRT18P6, 131 more genes
    nsv5189602mobile element insertion1nstd203human GRCh38 chr14: 33,948,057-33,948,071 , GRCh37.p13 chr14: 34,417,263-34,417,277 EGLN3
    nsv4729414copy number variation1nstd102humanUncertain significance GRCh37 chr14: 34,190,493-34,678,663 , GRCh38.p12 chr14: 33,721,287-34,209,457 LOC105370444, NPAS3, 4 more genes
    nsv4685750copy number variation1nstd102humannot provided GRCh37 chr14: 20,511,672-42,881,888 , GRCh38.p12 chr14: 20,043,513-42,412,685 IGBP1P1, RAB2B, 579 more genes
    nsv4675943copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-44,829,030 , GRCh38.p12 chr14: 20,043,513-44,359,827 TRAJ36, SEC23A-AS1, 590 more genes
    nsv4529244copy number variation1nstd166human GRCh37.p13 chr14: 34,365,399-34,817,000 , GRCh38.p12 chr14: 33,896,193-34,347,794 , EGLN3, 4 more genes
    nsv4457320copy number variation1nstd102humanPathogenic GRCh37 chr14: 30,448,939-35,017,859 , GRCh38.p12 chr14: 29,979,733-34,548,653 NARS1P1, RNU1-27P, 56 more genes
    nsv3924751copy number variation1nstd102humanPathogenic GRCh37 chr14: 31,261,477-45,154,334 , GRCh38 chr14: 30,792,271-44,685,131 , NCBI36 chr14: 30,331,228-44,224,084 DNAJC8P1, SNORA101B, 171 more genes
    nsv3922917copy number variation1nstd102humanPathogenic GRCh37 chr14: 30,851,760-38,181,546 , NCBI36 chr14: 29,921,511-37,251,297 , GRCh38 chr14: 30,382,554-37,712,341 MBIP, LOC105370447, 124 more genes
    nsv3921865copy number variation1nstd102humanUncertain significance NCBI36 chr14: 33,301,123-35,730,707 , GRCh37 chr14: 34,231,372-36,660,956 , GRCh38 chr14: 33,762,166-36,191,750 RPS19P3, LINC00609, 55 more genes
    nsv3919106copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482 SRMP2, IGHV3-71, 1929 more genes
    nsv3918965copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,490,852-44,562,875 , GRCh38 chr14: 20,022,693-44,093,672 , NCBI36 chr14: 19,560,692-43,632,625 TRAJ13, LRP10, 589 more genes
    nsv3917422copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478 MIR656, TRAJ59, 1918 more genes
    nsv3917157copy number variation1nstd102humanPathogenic GRCh37 chr14: 24,018,169-42,452,605 , GRCh38 chr14: 23,548,960-41,983,402 , NCBI36 chr14: 23,088,009-41,522,355 LINC02300, COCH, 274 more genes
    nsv3916277copy number variation1nstd102humanPathogenic NCBI36 chr14: 19,734,944-44,823,755 , GRCh38 chr14: 20,196,945-45,284,802 , GRCh37 chr14: 20,665,104-45,754,005 MIR208B, MRPL52, 600 more genes
    nsv3916173copy number variation1nstd102humanPathogenic NCBI36 chr14: 33,118,898-48,418,573 , GRCh37.p13 chr14: 34,049,147-49,348,823 , GRCh38.p12 chr14: 33,579,941-48,879,620 TTC6, LOC105370449, 178 more genes
    nsv3913204copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-49,111,245 , GRCh38 chr14: 20,043,513-48,642,042 , NCBI36 chr14: 19,581,512-48,180,995 SMARCE1P3, LOC100421646, 635 more genes
    nsv3912710copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,000,611-38,984,415 , NCBI36 chr14: 19,538,610-38,523,370 , GRCh37 chr14: 20,468,770-39,453,619 UBE2NP1, MIR4307HG, 553 more genes
    nsv3912538copy number variation1nstd102humanPathogenic GRCh37 chr14: 31,139,520-45,459,798 , GRCh38 chr14: 30,670,314-44,990,595 , NCBI36 chr14: 30,209,271-44,529,548 IGBP1P1, RPL9P3, 182 more genes
    nsv3912278copy number variation1nstd102humanPathogenic GRCh38 chr14: 33,880,412-42,359,485 , NCBI36 chr14: 33,419,369-41,898,438 , GRCh37 chr14: 34,349,618-42,828,688 RPL23AP8, LOC105370459, 120 more genes
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