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Items: 1 to 20 of 489

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5957141insertion1nstd209human GRCh38 chr4: 122,267,051-122,267,051 , GRCh37.p13 chr4: 123,188,206-123,188,206 BLTP1
    nsv5903746copy number variation1nstd209human GRCh38 chr4: 122,211,056-122,211,295 , GRCh37.p13 chr4: 123,132,211-123,132,450 BLTP1
    nsv5895495copy number variation1nstd209human GRCh38 chr4: 122,321,415-122,321,539 , GRCh37.p13 chr4: 123,242,570-123,242,694 BLTP1
    nsv5892922copy number variation1nstd209human GRCh38 chr4: 122,241,835-122,241,904 , GRCh37.p13 chr4: 123,162,990-123,163,059 BLTP1
    nsv5837873copy number variation1nstd209human GRCh38 chr4: 122,275,203-122,276,202 , GRCh37.p13 chr4: 123,196,358-123,197,357 BLTP1
    nsv5725477mobile element insertion1nstd211human GRCh38 chr4: 122,176,904-122,176,904 , GRCh37.p13 chr4: 123,098,059-123,098,059 BLTP1
    nsv5684620mobile element insertion2nstd211human GRCh38 chr4: 122,329,372-122,329,372 , GRCh37.p13 chr4: 123,250,527-123,250,527 BLTP1
    nsv5621288insertion1nstd207human GRCh38 chr4: 122,211,056-122,211,056 , GRCh37.p13 chr4: 123,132,211-123,132,211 BLTP1
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5558253sequence alteration1nstd206human GRCh38 chr4: 120,373,769-143,797,136 , GRCh37.p13 chr4: 121,294,924-144,718,289 , IL15, 218 more genes
    nsv5555251mobile element insertion1nstd206human GRCh38 chr4: 122,176,904-122,176,955 , GRCh37.p13 chr4: 123,098,059-123,098,110 BLTP1
    nsv5473360copy number variation1nstd206human GRCh38 chr4: 121,981,381-122,319,381 , GRCh37.p13 chr4: 122,902,536-123,240,536 BLTP1, LOC112268469, 2 more genes
    nsv5456389copy number variation1nstd206human GRCh38 chr4: 122,211,056-122,211,296 , GRCh37.p13 chr4: 123,132,211-123,132,451 BLTP1
    nsv5454533copy number variation1nstd206human GRCh38 chr4: 122,241,830-122,241,905 , GRCh37.p13 chr4: 123,162,985-123,163,060 BLTP1
    nsv5396928mobile element insertion1nstd206human GRCh38 chr4: 122,329,372-122,329,423 , GRCh37.p13 chr4: 123,250,527-123,250,578 BLTP1
    nsv5381774copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,833,638-130,232,122 , GRCh38.p12 chr4: 115,912,482-129,310,967 LOC112268469, LOC105377393, 159 more genes
    nsv5367801translocation1nstd200human GRCh38 chr4: 122,079,178-122,079,178 , GRCh38 chr4: 122,177,443-122,177,443 , GRCh37.p13 chr4: 123,098,598-123,098,598 , GRCh37.p13 chr4: 123,000,333-123,000,333 BLTP1
    nsv5342900translocation1nstd200human GRCh37 chr4: 123,000,333-123,000,333 , GRCh37 chr4: 123,098,598-123,098,598 , GRCh38.p12 chr4: 122,079,178-122,079,178 , GRCh38.p12 chr4: 122,177,443-122,177,443 BLTP1
    nsv5303754copy number variation1nstd204human GRCh38.p13 chr4: 122,211,046-122,211,305 , GRCh37.p13 chr4: 123,132,201-123,132,460 BLTP1
    nsv5225005copy number variation1nstd204human GRCh38.p13 chr4: 122,165,501-122,165,800 , GRCh37.p13 chr4: 123,086,656-123,086,955 BLTP1
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