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Items: 1 to 20 of 338

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969033inversion1nstd209human GRCh38 chr4: 108,267,752-117,667,772 , GRCh37.p13 chr4: 109,188,908-118,588,927 , ANK2, 134 more genes
    nsv5964786insertion1nstd209human GRCh38 chr4: 110,013,803-110,013,803 , GRCh37.p13 chr4: 110,934,959-110,934,959 EGF
    nsv5887994copy number variation1nstd209human GRCh38 chr4: 109,919,582-109,924,579 , GRCh37.p13 chr4: 110,840,738-110,845,735 EGF
    nsv5837289copy number variation1nstd209human GRCh38 chr4: 109,919,575-109,924,584 , GRCh37.p13 chr4: 110,840,731-110,845,740 EGF
    nsv5721134mobile element insertion2nstd211human GRCh38 chr4: 109,921,269-109,921,269 , GRCh37.p13 chr4: 110,842,425-110,842,425 EGF
    nsv5689907mobile element insertion2nstd211human GRCh38 chr4: 110,002,612-110,002,612 , GRCh37.p13 chr4: 110,923,768-110,923,768 EGF
    nsv5682944mobile element insertion1nstd211human GRCh38 chr4: 109,927,845-109,927,845 , GRCh37.p13 chr4: 110,849,001-110,849,001 EGF
    nsv5680730mobile element insertion2nstd211human GRCh38 chr4: 110,013,814-110,013,814 , GRCh37.p13 chr4: 110,934,970-110,934,970 EGF
    nsv5675765mobile element insertion1nstd211human GRCh38 chr4: 109,918,271-109,918,271 , GRCh37.p13 chr4: 110,839,427-110,839,427 EGF
    nsv5621690insertion1nstd207human GRCh38 chr4: 110,013,803-110,013,803 , GRCh37.p13 chr4: 110,934,959-110,934,959 EGF
    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
    nsv5539221insertion1nstd206human GRCh38 chr4: 109,921,269-109,921,304 , GRCh37.p13 chr4: 110,842,425-110,842,460 EGF
    nsv5471813copy number variation1nstd206human GRCh38 chr4: 109,919,584-109,924,580 , GRCh37.p13 chr4: 110,840,740-110,845,736 EGF
    nsv5467714copy number variation1nstd206human GRCh38 chr4: 109,924,963-109,925,869 , GRCh37.p13 chr4: 110,846,119-110,847,025 EGF
    nsv5412439mobile element insertion1nstd206human GRCh38 chr4: 110,002,612-110,002,663 , GRCh37.p13 chr4: 110,923,768-110,923,819 EGF
    nsv5409562mobile element insertion1nstd206human GRCh38 chr4: 110,013,803-110,013,803 , GRCh37.p13 chr4: 110,934,959-110,934,959 EGF
    nsv5311903copy number variation1nstd204human GRCh38.p13 chr4: 109,919,561-109,924,602 , GRCh37.p13 chr4: 110,840,717-110,845,758 EGF
    nsv5228319copy number variation1nstd204human GRCh38.p13 chr4: 109,919,601-109,924,600 , GRCh37.p13 chr4: 110,840,757-110,845,756 EGF
    nsv5222154copy number variation1nstd204human GRCh38.p13 chr4: 109,919,637-109,924,646 , GRCh37.p13 chr4: 110,840,793-110,845,802 EGF
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