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Items: 1 to 20 of 218

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054657inversion1nstd229human GRCh38 chr2: 18,305,934-19,842,483 , GRCh37.p13 chr2: 18,487,200-20,042,244 OSR1, CISD1P1, 14 more genes
    nsv6672575copy number variation1nstd229human GRCh38 chr2: 19,455,352-19,458,084 , GRCh37.p13 chr2: 19,655,113-19,657,845 LOC101928196
    nsv6669707copy number variation1nstd229human GRCh38 chr2: 19,424,401-19,434,800 , GRCh37.p13 chr2: 19,624,162-19,634,561 LOC105373458, LOC101928196
    nsv6668299copy number variation1nstd229human GRCh38 chr2: 19,404,097-19,407,367 , GRCh37.p13 chr2: 19,603,858-19,607,128 LOC101928196
    nsv6663705copy number variation1nstd229human GRCh38 chr2: 19,200,219-20,084,308 , GRCh37.p13 chr2: 19,399,980-20,284,069 WDR35-DT, LOC105373458, 14 more genes
    nsv6660744copy number variation1nstd229human GRCh38 chr2: 19,459,388-19,475,981 , GRCh37.p13 chr2: 19,659,149-19,675,742 LOC101928196, LINC01808
    nsv6660695copy number variation1nstd229human GRCh38 chr2: 19,406,886-19,407,989 , GRCh37.p13 chr2: 19,606,647-19,607,750 LOC101928196
    nsv6658923copy number variation1nstd229human GRCh38 chr2: 19,463,282-19,463,322 , GRCh37.p13 chr2: 19,663,043-19,663,083 LOC101928196
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6542859inversion1nstd223human GRCh38 chr2: 19,427,132-19,428,900 , GRCh37.p13 chr2: 19,626,893-19,628,661 LOC101928196, LOC105373458
    nsv6352960copy number variation1nstd223human GRCh38 chr2: 19,163,946-19,538,550 , GRCh37.p13 chr2: 19,363,707-19,738,311 LOC101928196, LOC105373458, 3 more genes
    nsv6348746copy number variation1nstd223human GRCh38 chr2: 19,433,967-19,434,372 , GRCh37.p13 chr2: 19,633,728-19,634,133 LOC105373458, LOC101928196
    nsv6347745copy number variation1nstd223human GRCh38 chr2: 19,455,417-19,459,071 , GRCh37.p13 chr2: 19,655,178-19,658,832 LOC101928196
    nsv6346455copy number variation1nstd223human GRCh38 chr2: 19,400,422-19,400,811 , GRCh37.p13 chr2: 19,600,183-19,600,572 LOC101928196
    nsv6342128copy number variation1nstd223human GRCh38 chr2: 19,200,219-20,084,308 , GRCh37.p13 chr2: 19,399,980-20,284,069 LAPTM4A-DT, LINC01808, 14 more genes
    nsv6340945copy number variation1nstd223human GRCh38 chr2: 19,416,521-20,093,799 , GRCh37.p13 chr2: 19,616,282-20,293,560 LOC105373459, LINC00954, 12 more genes
    nsv6337392copy number variation1nstd223human GRCh38 chr2: 19,399,201-19,400,700 , GRCh37.p13 chr2: 19,598,962-19,600,461 LOC101928196
    nsv6336274copy number variation1nstd223human GRCh38 chr2: 19,406,818-19,407,991 , GRCh37.p13 chr2: 19,606,579-19,607,752 LOC101928196
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
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