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Items: 1 to 20 of 943

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094799copy number variation1nstd102humanPathogenic GRCh37 chr16: 10,273,835-10,274,268 , GRCh38.p12 chr16: 10,179,978-10,180,411 GRIN2A
    nsv7094607copy number variation1nstd102humanUncertain significance GRCh37 chr16: 8,829,597-11,683,693 , GRCh38.p12 chr16: 8,735,740-11,589,837 LOC400499, NUBP1, 58 more genes
    nsv7094553copy number variation1nstd102humanPathogenic GRCh37 chr16: 10,031,796-10,032,428 , GRCh38.p12 chr16: 9,937,939-9,938,571 GRIN2A
    nsv7077104inversion1nstd229human GRCh38 chr16: 9,931,469-9,931,513 , GRCh37.p13 chr16: 10,025,326-10,025,370 GRIN2A
    nsv7076079inversion1nstd229human GRCh38 chr16: 9,015,595-14,846,246 , GRCh37.p13 chr16: 9,109,452-14,940,103 LOC105371093, RNU6-633P, 100 more genes
    nsv7074195inversion1nstd229human GRCh38 chr16: 9,923,547-9,930,080 , GRCh37.p13 chr16: 10,017,404-10,023,937 GRIN2A
    nsv7073287inversion1nstd229human GRCh38 chr16: 9,861,285-9,866,392 , GRCh37.p13 chr16: 9,955,142-9,960,249 GRIN2A
    nsv7066090inversion1nstd229human GRCh38 chr16: 9,925,182-9,932,178 , GRCh37.p13 chr16: 10,019,039-10,026,035 GRIN2A
    nsv7065073inversion1nstd229human GRCh38 chr16: 9,996,504-10,008,706 , GRCh37.p13 chr16: 10,090,361-10,102,563 GRIN2A
    nsv7061543inversion1nstd229human GRCh38 chr16: 9,947,132-9,958,957 , GRCh37.p13 chr16: 10,040,989-10,052,814 GRIN2A
    nsv7059417inversion1nstd229human GRCh38 chr16: 10,012,413-10,013,931 , GRCh37.p13 chr16: 10,106,270-10,107,788 GRIN2A
    nsv6977179copy number variation1nstd229human GRCh38 chr16: 10,106,501-10,106,550 , GRCh37.p13 chr16: 10,200,358-10,200,407 GRIN2A
    nsv6977168copy number variation1nstd229human GRCh38 chr16: 10,089,598-10,137,440 , GRCh37.p13 chr16: 10,183,455-10,231,297 IMPDH1P11, GRIN2A
    nsv6976304copy number variation1nstd229human GRCh38 chr16: 10,001,724-10,057,331 , GRCh37.p13 chr16: 10,095,581-10,151,188 LOC105371076, GRIN2A
    nsv6976211copy number variation1nstd229human GRCh38 chr16: 10,128,584-10,129,487 , GRCh37.p13 chr16: 10,222,441-10,223,344 GRIN2A
    nsv6975701copy number variation1nstd229human GRCh38 chr16: 10,041,772-10,111,365 , GRCh37.p13 chr16: 10,135,629-10,205,222 GRIN2A, IMPDH1P11
    nsv6974645copy number variation1nstd229human GRCh38 chr16: 9,976,863-10,068,019 , GRCh37.p13 chr16: 10,070,720-10,161,876 LOC105371076, GRIN2A
    nsv6974503copy number variation1nstd229human GRCh38 chr16: 9,926,001-9,933,800 , GRCh37.p13 chr16: 10,019,858-10,027,657 GRIN2A
    nsv6974306copy number variation1nstd229human GRCh38 chr16: 10,073,504-10,076,445 , GRCh37.p13 chr16: 10,167,361-10,170,302 GRIN2A
    nsv6973522copy number variation1nstd229human GRCh38 chr16: 9,868,868-9,883,180 , GRCh37.p13 chr16: 9,962,725-9,977,037 GRIN2A
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