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Items: 1 to 20 of 74

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5560388sequence alteration1nstd206human GRCh38 chr14: 32,201,749-32,203,441 , GRCh37.p13 chr14: 32,670,955-32,672,647 AKAP6, RNU6-7, 1 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
    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
    nsv4455578copy number variation1nstd102humanUncertain significance GRCh37 chr14: 32,464,298-32,767,649 , GRCh38.p12 chr14: 31,995,092-32,298,443 ARHGAP5-AS1, LOC100533787, 6 more genes
    nsv4227591copy number variation1nstd166human GRCh37.p13 chr14: 32,647,313-32,693,091 , GRCh38.p12 chr14: 32,178,107-32,223,885 RNU6-8, RNU6-7, 1 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
    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
    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
    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
    nsv3911062copy number variation1nstd102humanPathogenic GRCh37 chr14: 29,273,194-33,703,472 , NCBI36 chr14: 28,342,945-32,773,223 , GRCh38 chr14: 28,803,988-33,234,266 HEATR5A, LOC100506071, 54 more genes
    nsv3907460copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456 BANF1P1, IGHV1-68, 1996 more genes
    nsv3904265copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229 CRIP1, GPATCH2L, 1929 more genes
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