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Items: 1 to 20 of 274

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960130insertion1nstd209human GRCh38 chr8: 106,783,017-106,783,017 , GRCh37.p13 chr8: 107,795,245-107,795,245 ABRA
    nsv5923523copy number variation1nstd209human GRCh38 chr8: 106,771,137-106,775,800 , GRCh37.p13 chr8: 107,783,365-107,788,028 ABRA
    nsv5850850copy number variation1nstd209human GRCh38 chr8: 106,770,106-106,771,295 , GRCh37.p13 chr8: 107,782,334-107,783,523 ABRA
    nsv5847604copy number variation1nstd209human GRCh38 chr8: 106,771,184-106,775,412 , GRCh37.p13 chr8: 107,783,412-107,787,640 ABRA
    nsv5643653insertion1nstd207human GRCh38 chr8: 106,783,070-106,783,070 , GRCh37.p13 chr8: 107,795,298-107,795,298 ABRA
    nsv5544094insertion1nstd206human GRCh38 chr8: 106,783,064-106,783,116 , GRCh37.p13 chr8: 107,795,292-107,795,344 ABRA
    nsv5541631insertion1nstd206human GRCh38 chr8: 106,783,062-106,783,100 , GRCh37.p13 chr8: 107,795,290-107,795,328 ABRA
    nsv5491802copy number variation1nstd206human GRCh38 chr8: 106,758,033-106,758,796 , GRCh37.p13 chr8: 107,770,261-107,771,024 ABRA
    nsv5474121copy number variation1nstd206human GRCh38 chr8: 106,771,139-106,775,802 , GRCh37.p13 chr8: 107,783,367-107,788,030 ABRA
    nsv5372088translocation1nstd200human GRCh38 chr8: 106,764,941-106,764,941 , GRCh38 chr8: 106,764,857-106,764,857 , GRCh37.p13 chr8: 107,777,169-107,777,169 , GRCh37.p13 chr8: 107,777,085-107,777,085 ABRA
    nsv5364321translocation1nstd200human GRCh38 chr8: 90,443,448-90,443,448 , GRCh38 chr8: 106,789,724-106,789,724 , GRCh37.p13 chr8: 91,455,676-91,455,676 , GRCh37.p13 chr8: 107,801,952-107,801,952 ABRA
    nsv5364320translocation1nstd200human GRCh38 chr8: 90,438,676-90,438,676 , GRCh38 chr8: 106,789,733-106,789,733 , GRCh37.p13 chr8: 107,801,961-107,801,961 , GRCh37.p13 chr8: 91,450,904-91,450,904 ABRA
    nsv5319974copy number variation1nstd204human GRCh38.p13 chr8: 106,771,153-106,775,764 , GRCh37.p13 chr8: 107,783,381-107,787,992 ABRA
    nsv5244775copy number variation1nstd204human GRCh38.p13 chr8: 106,773,001-106,774,900 , GRCh37.p13 chr8: 107,785,229-107,787,128 ABRA
    nsv5244491copy number variation1nstd204human GRCh38.p13 chr8: 106,771,201-106,783,100 , GRCh37.p13 chr8: 107,783,429-107,795,328 ABRA
    nsv5240478copy number variation1nstd204human GRCh38.p13 chr8: 106,770,856-106,775,712 , GRCh37.p13 chr8: 107,783,084-107,787,940 ABRA
    nsv5039005inversion1nstd200human GRCh38 chr8: 102,793,534-107,480,712 , GRCh37.p13 chr8: 103,805,762-108,492,940 , LOC105375693, 58 more genes
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4961750copy number variation1nstd200human GRCh38 chr8: 106,771,164-106,775,745 , GRCh37.p13 chr8: 107,783,392-107,787,973 ABRA
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