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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976348inversion1nstd209human GRCh38 chr4: 103,823,749-108,603,414 , GRCh37.p13 chr4: 104,744,906-109,524,570 , HADH, 54 more genes
    nsv5903439copy number variation1nstd209human GRCh38 chr4: 106,321,438-106,321,514 , GRCh37.p13 chr4: 107,242,595-107,242,671 AIMP1
    nsv5902011copy number variation1nstd209human GRCh38 chr4: 106,299,142-106,345,993 , GRCh37.p13 chr4: 107,220,299-107,267,150 AIMP1, TBCK
    nsv5837552copy number variation1nstd209human GRCh38 chr4: 106,327,101-106,345,474 , GRCh37.p13 chr4: 107,248,258-107,266,631 AIMP1
    nsv5837551copy number variation1nstd209human GRCh38 chr4: 106,322,415-106,326,450 , GRCh37.p13 chr4: 107,243,572-107,247,607 AIMP1
    nsv5837550copy number variation1nstd209human GRCh38 chr4: 106,299,179-106,320,620 , GRCh37.p13 chr4: 107,220,336-107,241,777 TBCK, AIMP1
    nsv5581419copy number variation1nstd207human GRCh38 chr4: 106,321,438-106,321,514 , GRCh37.p13 chr4: 107,242,595-107,242,671 AIMP1
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5471224copy number variation1nstd206human GRCh38 chr4: 106,321,462-106,321,515 , GRCh37.p13 chr4: 107,242,619-107,242,672 AIMP1
    nsv5471177copy number variation1nstd206human GRCh38 chr4: 106,344,828-106,344,910 , GRCh37.p13 chr4: 107,265,985-107,266,067 AIMP1
    nsv5464988copy number variation1nstd206human GRCh38 chr4: 106,340,126-106,340,980 , GRCh37.p13 chr4: 107,261,283-107,262,137 AIMP1
    nsv5312769copy number variation1nstd204human GRCh38.p13 chr4: 106,319,706-106,321,898 , GRCh37.p13 chr4: 107,240,863-107,243,055 AIMP1
    nsv5234320copy number variation1nstd204human GRCh38.p13 chr4: 106,319,801-106,322,100 , GRCh37.p13 chr4: 107,240,958-107,243,257 AIMP1
    nsv5232461copy number variation1nstd204human GRCh38.p13 chr4: 106,319,771-106,321,964 , GRCh37.p13 chr4: 107,240,928-107,243,121 AIMP1
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4935119copy number variation1nstd200human GRCh38 chr4: 106,321,326-106,321,394 , GRCh37.p13 chr4: 107,242,483-107,242,551 AIMP1
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4801022copy number variation1nstd200human GRCh37 chr4: 107,240,892-107,243,032 , GRCh38.p12 chr4: 106,319,735-106,321,875 AIMP1
    nsv4801019copy number variation1nstd200human GRCh37 chr4: 107,062,393-107,237,190 , GRCh38.p12 chr4: 106,141,236-106,316,033 AIMP1, TBCK
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