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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5911839copy number variation1nstd209human GRCh38 chr9: 97,998,776-97,999,105 , GRCh37.p13 chr9: 100,761,058-100,761,387 ANP32B
    nsv5911662copy number variation1nstd209human GRCh38 chr9: 98,012,014-98,012,139 , GRCh37.p13 chr9: 100,774,296-100,774,421 ANP32B
    nsv5588874copy number variation1nstd207human GRCh38 chr9: 97,998,776-97,999,105 , GRCh37.p13 chr9: 100,761,058-100,761,387 ANP32B
    nsv5480931copy number variation1nstd206human GRCh38 chr9: 97,998,793-97,999,106 , GRCh37.p13 chr9: 100,761,075-100,761,388 ANP32B
    nsv5384459mobile element deletion2nstd186human GRCh37 chr9: 100,761,075-100,761,388 , GRCh38.p12 chr9: 97,998,793-97,999,106 ANP32B
    nsv5381561copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807 TBC1D2, ZNF782, 170 more genes
    nsv5245259copy number variation1nstd204human GRCh38.p13 chr9: 97,999,167-98,001,466 , GRCh37.p13 chr9: 100,761,449-100,763,748 ANP32B
    nsv5215989mobile element deletion1nstd204human GRCh38.p13 chr9: 97,998,793-97,999,106 , GRCh37.p13 chr9: 100,761,075-100,761,388 ANP32B
    nsv5127394mobile element insertion1nstd203human GRCh38 chr9: 97,985,781-97,985,799 , GRCh37.p13 chr9: 100,748,063-100,748,081 ANP32B
    nsv4893480mobile element deletion1nstd200human GRCh38 chr9: 97,998,793-97,999,106 , GRCh37.p13 chr9: 100,761,075-100,761,388 ANP32B
    nsv4771252mobile element deletion1nstd200human GRCh37 chr9: 100,761,075-100,761,388 , GRCh38.p12 chr9: 97,998,793-97,999,106 ANP32B
    nsv4748695copy number variation1nstd199human GRCh37 chr9: 100,761,062-100,761,392 , GRCh38.p12 chr9: 97,998,780-97,999,110 ANP32B
    nsv4711317copy number variation4nstd195human GRCh37 chr9: 100,761,058-100,761,059 , GRCh38.p12 chr9: 97,998,776-97,998,777 ANP32B
    nsv4684256copy number variation1nstd102humanPathogenic GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991 RPS26P37, MIR27B, 238 more genes
    nsv4683944copy number variation1nstd102humanUncertain significance GRCh37 chr9: 100,190,728-101,558,793 , GRCh38.p12 chr9: 97,428,446-98,796,511 TRMO, RNU6-918P, 20 more genes
    nsv4676103copy number variation1nstd102humanPathogenic NCBI36 chr9: 95,946,863-99,986,314 , GRCh37.p13 chr9: 96,907,042-100,946,493 , GRCh38.p12 chr9: 94,144,760-98,184,211 MIR3074, LOC112268039, 108 more genes
    nsv4653803mobile element deletion1nstd186human GRCh37 chr9: 100,761,059-100,761,388 , GRCh38.p12 chr9: 97,998,777-97,999,106 ANP32B
    nsv4638488copy number variation1nstd186human GRCh37 chr9: 100,761,075-100,761,388 , GRCh38.p12 chr9: 97,998,793-97,999,106 ANP32B
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
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