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Items: 1 to 20 of 87

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6957819copy number variation1nstd229human GRCh38 chr14: 29,967,815-31,229,292 , GRCh37.p13 chr14: 30,437,021-31,698,498 LOC100913082, RPS6P24, 19 more genes
    nsv6952773copy number variation1nstd229human GRCh38 chr14: 30,780,825-30,808,630 , GRCh37.p13 chr14: 31,250,031-31,277,836 RPL12P5
    nsv6944468copy number variation1nstd229human GRCh38 chr14: 30,786,624-30,796,667 , GRCh37.p13 chr14: 31,255,830-31,265,873 RPL12P5
    nsv6637416copy number variation1nstd102humanPathogenic GRCh37 chr14: 24,959,823-33,415,359 , GRCh38.p12 chr14: 24,490,617-32,946,153 SCFD1, RPL12P5, 94 more genes
    nsv6591606inversion1nstd223human GRCh38 chr14: 30,656,873-33,818,146 , GRCh37.p13 chr14: 31,126,079-34,287,352 ARHGAP5-AS1, RN7SL660P, 37 more genes
    nsv6484862copy number variation1nstd223human GRCh38 chr14: 30,786,622-30,796,666 , GRCh37.p13 chr14: 31,255,828-31,265,872 RPL12P5
    nsv6315513copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-47,481,203 , GRCh38.p12 chr14: 20,043,513-47,012,000 CDH24, KLHL33, 623 more genes
    nsv6314715copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884 HNRNPC, FOXG1, 616 more genes
    nsv6132586copy number variation1nstd213human GRCh37 chr14: 31,100,000-31,670,001 , GRCh38.p12 chr14: 30,630,794-31,200,795 AP4S1, UBE2CP1, 12 more genes
    nsv5932850copy number variation1nstd209human GRCh38 chr14: 30,786,693-30,796,606 , GRCh37.p13 chr14: 31,255,899-31,265,812 RPL12P5
    nsv5859309copy number variation1nstd209human GRCh38 chr14: 30,785,995-30,793,156 , GRCh37.p13 chr14: 31,255,201-31,262,362 RPL12P5
    nsv5381770copy number variation1nstd102humanPathogenic GRCh37 chr14: 27,450,705-31,529,481 , GRCh38.p12 chr14: 26,981,499-31,060,275 RPS27AP4, LINC00645, 43 more genes
    nsv4991102copy number variation1nstd200human GRCh38 chr14: 30,786,622-30,796,666 , GRCh37.p13 chr14: 31,255,828-31,265,872 RPL12P5
    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
    nsv4624666copy number variation1nstd183human GRCh37 chr14: 30,782,367-31,539,196 , GRCh38.p12 chr14: 30,313,161-31,069,990 AP4S1, G2E3-AS1, 15 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
    nsv4218492copy number variation1nstd166human GRCh37.p13 chr14: 31,255,829-31,265,872 , GRCh38.p12 chr14: 30,786,623-30,796,666 RPL12P5
    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
    nsv3922163copy number variation1nstd102humanPathogenic NCBI36 chr14: 26,243,854-32,957,356 , GRCh37.p13 chr14: 27,174,014-33,887,605 , GRCh38.p12 chr14: 26,704,808-33,418,399 LINC02293, ARHGAP5, 77 more genes
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