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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099244copy number variation1nstd231human GRCh38.p12 chr1: 166,864,890-169,028,321 , GRCh37 chr1: 166,834,127-168,997,559 CD247, DPT, 49 more genes
    nsv7095709copy number variation1nstd102humanPathogenic GRCh37 chr1: 167,487,625-167,487,702 , GRCh38.p12 chr1: 167,518,388-167,518,465 CD247, AKR1D1P1
    nsv7095708copy number variation1nstd102humanUncertain significance GRCh37 chr1: 167,400,918-167,410,024 , GRCh38.p12 chr1: 167,431,681-167,440,787 CD247
    nsv7095561copy number variation1nstd102humanUncertain significance GRCh37 chr1: 167,400,918-168,282,240 , GRCh38.p12 chr1: 167,431,681-168,313,002 GCSHP5, RNU6-1310P, 21 more genes
    nsv7057094inversion1nstd229human GRCh38 chr1: 167,478,851-167,506,118 , GRCh37.p13 chr1: 167,448,088-167,475,355 CD247
    nsv7047642inversion1nstd229human GRCh38 chr1: 167,459,752-167,504,189 , GRCh37.p13 chr1: 167,428,989-167,473,426 CD247
    nsv7039884inversion1nstd229human GRCh38 chr1: 159,817,036-167,858,499 , GRCh37.p13 chr1: 159,786,826-167,827,737 TRP-AGG2-1, FCGR2C, 228 more genes
    nsv6644239copy number variation1nstd229human GRCh38 chr1: 167,270,558-167,699,449 , GRCh37.p13 chr1: 167,239,795-167,668,686 POU2F1, LOC101928512, 6 more genes
    nsv6644188copy number variation1nstd229human GRCh38 chr1: 167,512,347-167,512,487 , GRCh37.p13 chr1: 167,481,584-167,481,724 CD247
    nsv6644187copy number variation1nstd229human GRCh38 chr1: 167,464,801-167,472,400 , GRCh37.p13 chr1: 167,434,038-167,441,637 CD247
    nsv6644186copy number variation1nstd229human GRCh38 chr1: 167,449,688-167,453,689 , GRCh37.p13 chr1: 167,418,925-167,422,926 CD247, LOC101928512
    nsv6644184copy number variation1nstd229human GRCh38 chr1: 167,392,871-167,445,339 , GRCh37.p13 chr1: 167,362,108-167,414,576 POU2F1, CD247
    nsv6644128copy number variation1nstd229human GRCh38 chr1: 167,485,955-167,491,186 , GRCh37.p13 chr1: 167,455,192-167,460,423 CD247
    nsv6644127copy number variation1nstd229human GRCh38 chr1: 167,482,901-167,493,400 , GRCh37.p13 chr1: 167,452,138-167,462,637 CD247
    nsv6644126copy number variation1nstd229human GRCh38 chr1: 167,457,181-167,461,598 , GRCh37.p13 chr1: 167,426,418-167,430,835 CD247, LOC101928512
    nsv6644125copy number variation1nstd229human GRCh38 chr1: 167,444,181-167,447,325 , GRCh37.p13 chr1: 167,413,418-167,416,562 CD247
    nsv6643752copy number variation1nstd229human GRCh38 chr1: 167,489,896-167,495,067 , GRCh37.p13 chr1: 167,459,133-167,464,304 CD247
    nsv6643750copy number variation1nstd229human GRCh38 chr1: 167,460,076-167,481,589 , GRCh37.p13 chr1: 167,429,313-167,450,826 CD247
    nsv6643749copy number variation1nstd229human GRCh38 chr1: 167,457,550-167,516,726 , GRCh37.p13 chr1: 167,426,787-167,485,963 CD247, LOC101928512
    nsv6554712inversion1nstd223human GRCh38 chr1: 167,459,140-167,459,641 , GRCh37.p13 chr1: 167,428,377-167,428,878 CD247, LOC101928512
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