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Items: 1 to 20 of 313

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 LOC105377327, LOC105377324, 214 more genes
    nsv7137046copy number variation1nstd102humanPathogenic GRCh38.p12 chr4: 89,247,780-89,953,418 , GRCh37 chr4: 90,168,931-90,874,569 SNCA, MMRN1, 4 more genes
    nsv7046112inversion1nstd229human GRCh38 chr4: 88,874,421-89,490,956 , GRCh37.p13 chr4: 89,795,572-90,412,107 GPRIN3, LOC105377328, 4 more genes
    nsv6757592copy number variation1nstd229human GRCh38 chr4: 89,252,200-89,560,372 , GRCh37.p13 chr4: 90,173,351-90,481,523 GPRIN3, LOC105377328, 1 more genes
    nsv6756506copy number variation1nstd229human GRCh38 chr4: 89,280,378-89,286,912 , GRCh37.p13 chr4: 90,201,529-90,208,063 GPRIN3
    nsv6755911copy number variation1nstd229human GRCh38 chr4: 89,291,067-89,299,992 , GRCh37.p13 chr4: 90,212,218-90,221,143 GPRIN3
    nsv6753996copy number variation1nstd229human GRCh38 chr4: 89,212,001-89,347,400 , GRCh37.p13 chr4: 90,133,152-90,268,551 GPRIN3
    nsv6753201copy number variation1nstd229human GRCh38 chr4: 89,227,791-89,277,001 , GRCh37.p13 chr4: 90,148,942-90,198,152 GPRIN3
    nsv6753129copy number variation1nstd229human GRCh38 chr4: 89,276,818-89,300,441 , GRCh37.p13 chr4: 90,197,969-90,221,592 GPRIN3
    nsv6752327copy number variation1nstd229human GRCh38 chr4: 88,105,357-91,750,216 , GRCh37.p13 chr4: 89,026,509-92,671,367 HERC5, SNCA, 34 more genes
    nsv6750423copy number variation1nstd229human GRCh38 chr4: 89,287,182-89,287,777 , GRCh37.p13 chr4: 90,208,333-90,208,928 GPRIN3
    nsv6750084copy number variation1nstd229human GRCh38 chr4: 89,266,378-89,289,356 , GRCh37.p13 chr4: 90,187,529-90,210,507 GPRIN3
    nsv6748673copy number variation1nstd229human GRCh38 chr4: 89,292,091-89,308,669 , GRCh37.p13 chr4: 90,213,242-90,229,820 GPRIN3
    nsv6745881copy number variation1nstd229human GRCh38 chr4: 89,289,234-89,586,576 , GRCh37.p13 chr4: 90,210,385-90,507,727 LOC105377329, GPRIN3, 1 more genes
    nsv6745057copy number variation1nstd229human GRCh38 chr4: 89,294,525-89,295,425 , GRCh37.p13 chr4: 90,215,676-90,216,576 GPRIN3
    nsv6744868copy number variation1nstd229human GRCh38 chr4: 89,302,180-89,302,397 , GRCh37.p13 chr4: 90,223,331-90,223,548 GPRIN3
    nsv6739311copy number variation1nstd229human GRCh38 chr4: 89,240,943-89,242,007 , GRCh37.p13 chr4: 90,162,094-90,163,158 GPRIN3
    nsv6739251copy number variation1nstd229human GRCh38 chr4: 89,239,124-89,248,677 , GRCh37.p13 chr4: 90,160,275-90,169,828 GPRIN3
    nsv6738755copy number variation1nstd229human GRCh38 chr4: 89,273,739-89,297,270 , GRCh37.p13 chr4: 90,194,890-90,218,421 GPRIN3
    nsv6629794copy number variation1nstd224human GRCh37 chr4: 90,198,463-90,216,747 , GRCh38.p12 chr4: 89,277,312-89,295,596 GPRIN3
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