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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5951492copy number variation1nstd209human GRCh38 chr22: 24,669,873-24,714,153 , GRCh37.p13 chr22: 25,065,840-25,110,120 ARL5AP4, CRIP1P4, 2 more genes
    nsv5543707copy number variation1nstd206human GRCh38 chr22: 24,669,493-24,714,097 , GRCh37.p13 chr22: 25,065,460-25,110,064 CRIP1P4, ARL5AP4, 2 more genes
    nsv5375631translocation1nstd200human GRCh38 chr22: 24,713,107-24,713,107 , GRCh38 chr22: 24,717,199-24,717,199 , GRCh37.p13 chr22: 25,113,166-25,113,166 , GRCh37.p13 chr22: 25,109,074-25,109,074 PIWIL3, CRIP1P4
    nsv5032291copy number variation1nstd200human GRCh38 chr22: 24,669,876-24,714,108 , GRCh37.p13 chr22: 25,065,843-25,110,075 CRIP1P4, ARL5AP4, 2 more genes
    nsv4768383copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-26,483,608 , GRCh38.p12 chr22: 16,408,173-26,087,642 KRT18P62, LOC101060852, 437 more genes
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4680763copy number variation1nstd189human GRCh37.p13 chr22: 24,891,356-26,623,160 , GRCh38.p12 chr22: 24,495,388-26,227,194 , GRK3, 37 more genes
    nsv4680353copy number variation1nstd189human GRCh37.p13 chr22: 25,013,443-25,483,921 , GRCh38.p12 chr22: 24,617,476-25,087,954 GGT1, TOP1P2, 10 more genes
    nsv4676422copy number variation1nstd102humanUncertain significance GRCh37 chr22: 24,311,474-26,075,188 , GRCh38.p12 chr22: 24,013,510-25,679,221 SPECC1L, LOC105372969, 39 more genes
    nsv4676211copy number variation1nstd102humanPathogenic GRCh37 chr22: 20,732,808-25,193,541 , GRCh38.p12 chr22: 20,378,518-24,797,574 IGLV3-16, ASH2LP2, 266 more genes
    nsv4676144copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-27,657,507 , GRCh38.p12 chr22: 16,408,173-27,261,546 LINC02891, IGLV4-69, 466 more genes
    nsv4627427copy number variation1nstd183human GRCh37 chr22: 25,065,840-25,110,121 , GRCh38.p12 chr22: 24,669,873-24,714,154 CRIP1P4, ARL5AP4, 2 more genes
    nsv4624661copy number variation1nstd183human GRCh37 chr22: 25,070,067-25,106,411 , GRCh38.p12 chr22: 24,674,100-24,710,444 LOC105372962, CRIP1P4, 2 more genes
    nsv4621861copy number variation1nstd183human GRCh37 chr22: 25,102,007-25,246,398 , GRCh38.p12 chr22: 24,706,040-24,850,431 TOP1P2, PIWIL3, 3 more genes
    nsv4457771copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410 IGLV3-27, XKR3, 1082 more genes
    nsv4457548copy number variation1nstd102humanPathogenic GRCh37 chr22: 22,962,196-25,145,601 , GRCh38.p12 chr22: 22,619,726-24,749,634 IGLV3-10, IGLV3-15, 128 more genes
    nsv4436798copy number variation1nstd102humanLikely pathogenic GRCh37 chr22: 22,963,000-25,130,055 , GRCh38.p12 chr22: 22,620,530-24,734,088 ADORA2A, ASLP1, 128 more genes
    nsv4415075copy number variation1nstd174human GRCh37 chr22: 25,065,655-25,110,121 , GRCh38.p12 chr22: 24,669,688-24,714,154 LOC105372962, ARL5AP4, 2 more genes
    nsv4383389copy number variation1nstd173human GRCh37 chr22: 21,465,662-33,984,045 , GRCh38.p12 chr22: 21,111,373-33,588,059 , XBP1, 450 more genes
    nsv4380454copy number variation1nstd173human GRCh37 chr22: 25,066,472-25,113,330 , GRCh38.p12 chr22: 24,670,505-24,717,363 CRIP1P4, LOC105372962, 3 more genes
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