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Items: 1 to 20 of 735

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5894158copy number variation1nstd209human GRCh38 chr4: 118,204,256-118,209,043 , GRCh37.p13 chr4: 119,125,411-119,130,198 NDST3
    nsv5894101copy number variation1nstd209human GRCh38 chr4: 118,103,801-118,104,095 , GRCh37.p13 chr4: 119,024,956-119,025,250 NDST3, LOC107986307
    nsv5837859copy number variation1nstd209human GRCh38 chr4: 118,204,290-118,209,022 , GRCh37.p13 chr4: 119,125,445-119,130,177 NDST3
    nsv5837858copy number variation1nstd209human GRCh38 chr4: 118,149,809-118,151,594 , GRCh37.p13 chr4: 119,070,964-119,072,749 NDST3
    nsv5837857copy number variation1nstd209human GRCh38 chr4: 118,148,549-118,150,280 , GRCh37.p13 chr4: 119,069,704-119,071,435 NDST3
    nsv5716378mobile element insertion1nstd211human GRCh38 chr4: 118,151,533-118,151,533 , GRCh37.p13 chr4: 119,072,688-119,072,688 NDST3
    nsv5714826mobile element insertion2nstd211human GRCh38 chr4: 118,121,028-118,121,028 , GRCh37.p13 chr4: 119,042,183-119,042,183 NDST3, LOC107986307
    nsv5686286mobile element insertion2nstd211human GRCh38 chr4: 118,197,694-118,197,694 , GRCh37.p13 chr4: 119,118,849-119,118,849 NDST3
    nsv5682150mobile element insertion1nstd211human GRCh38 chr4: 118,041,927-118,041,927 , GRCh37.p13 chr4: 118,963,082-118,963,082 NDST3
    nsv5679597mobile element insertion2nstd211human GRCh38 chr4: 118,190,988-118,190,988 , GRCh37.p13 chr4: 119,112,143-119,112,143 FKBP4P1, NDST3
    nsv5615917insertion1nstd207human GRCh38 chr4: 118,197,683-118,197,683 , GRCh37.p13 chr4: 119,118,838-119,118,838 NDST3
    nsv5578224copy number variation1nstd207human GRCh38 chr4: 118,066,709-118,066,777 , GRCh37.p13 chr4: 118,987,864-118,987,932 NDST3, LOC107986307
    nsv5578177copy number variation1nstd207human GRCh38 chr4: 118,066,495-118,066,713 , GRCh37.p13 chr4: 118,987,650-118,987,868 LOC107986307, NDST3
    nsv5571182copy number variation1nstd207human GRCh38 chr4: 118,204,256-118,209,043 , GRCh37.p13 chr4: 119,125,411-119,130,198 NDST3
    nsv5569436copy number variation1nstd207human GRCh38 chr4: 118,066,277-118,066,347 , GRCh37.p13 chr4: 118,987,432-118,987,502 LOC107986307, NDST3
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5559994mobile element insertion1nstd206human GRCh38 chr4: 118,151,483-118,151,533 , GRCh37.p13 chr4: 119,072,638-119,072,688 NDST3
    nsv5555919mobile element insertion1nstd206human GRCh38 chr4: 118,121,028-118,121,079 , GRCh37.p13 chr4: 119,042,183-119,042,234 NDST3, LOC107986307
    nsv5550255insertion1nstd206human GRCh38 chr4: 118,041,927-118,041,978 , GRCh37.p13 chr4: 118,963,082-118,963,133 NDST3
    nsv5545527insertion1nstd206human GRCh38 chr4: 118,197,683-118,197,683 , GRCh37.p13 chr4: 119,118,838-119,118,838 NDST3
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