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Items: 1 to 20 of 99

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066954inversion1nstd229human GRCh38 chr14: 30,982,854-31,221,335 , GRCh37.p13 chr14: 31,452,060-31,690,541 HECTD1, STRN3, 5 more genes
    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
    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
    nsv6584608inversion1nstd223human GRCh38 chr14: 30,982,854-31,221,335 , GRCh37.p13 chr14: 31,452,060-31,690,541 AP4S1, HECTD1, 5 more genes
    nsv6487752copy number variation1nstd223human GRCh38 chr14: 31,011,844-31,014,602 , GRCh37.p13 chr14: 31,481,050-31,483,808 STRN3, MIR624
    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
    nsv6130798insertion1nstd186human GRCh37 chr14: 31,483,140-31,483,146 , GRCh38.p12 chr14: 31,013,934-31,013,940 MIR624, STRN3
    nsv5545376insertion1nstd206human GRCh38 chr14: 31,013,934-31,013,940 , GRCh37.p13 chr14: 31,483,140-31,483,146 STRN3, MIR624
    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
    nsv4991118copy number variation1nstd200human GRCh38 chr14: 31,011,844-31,014,602 , GRCh37.p13 chr14: 31,481,050-31,483,808 MIR624, STRN3
    nsv4844771copy number variation1nstd200human GRCh37 chr14: 31,481,049-31,483,808 , GRCh38.p12 chr14: 31,011,843-31,014,602 STRN3, MIR624
    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
    nsv4632024copy number variation1nstd183human GRCh37 chr14: 31,483,770-31,484,032 , GRCh38.p12 chr14: 31,014,564-31,014,826 STRN3, MIR624
    nsv4627143copy number variation1nstd183human GRCh37 chr14: 31,479,845-31,483,971 , GRCh38.p12 chr14: 31,010,639-31,014,765 STRN3, MIR624
    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
    nsv4623536copy number variation1nstd183human GRCh37 chr14: 31,483,839-31,484,032 , GRCh38.p12 chr14: 31,014,633-31,014,826 STRN3, MIR624
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