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Items: 1 to 20 of 429

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977899inversion1nstd209human GRCh38 chr2: 227,539,323-230,369,909 , GRCh37.p13 chr2: 228,404,039-231,234,624 , AGFG1, 40 more genes
    nsv5948562insertion1nstd209human GRCh38 chr2: 228,139,910-228,139,910 , GRCh37.p13 chr2: 229,004,626-229,004,626 SPHKAP
    nsv5891011copy number variation1nstd209human GRCh38 chr2: 228,142,437-228,395,874 , GRCh37.p13 chr2: 229,007,153-229,260,590 SPHKAP, SNF8P1, 2 more genes
    nsv5832767copy number variation1nstd209human GRCh38 chr2: 228,079,640-228,081,668 , GRCh37.p13 chr2: 228,944,356-228,946,384 SPHKAP
    nsv5832529copy number variation1nstd209human GRCh38 chr2: 228,057,782-228,060,031 , GRCh37.p13 chr2: 228,922,498-228,924,747 SPHKAP
    nsv5832229copy number variation1nstd209human GRCh38 chr2: 228,142,404-228,207,489 , GRCh37.p13 chr2: 229,007,120-229,072,205 LOC107985993, SPHKAP, 1 more genes
    nsv5723351mobile element insertion1nstd211human GRCh38 chr2: 228,015,871-228,015,871 , GRCh37.p13 chr2: 228,880,587-228,880,587 SPHKAP, LOC105373918
    nsv5691658mobile element insertion2nstd211human GRCh38 chr2: 227,992,889-227,992,889 , GRCh37.p13 chr2: 228,857,605-228,857,605 SPHKAP, LOC105373918
    nsv5690965mobile element insertion1nstd211human GRCh38 chr2: 228,128,492-228,128,492 , GRCh37.p13 chr2: 228,993,208-228,993,208 SPHKAP
    nsv5680629mobile element insertion2nstd211human GRCh38 chr2: 227,981,230-227,981,230 , GRCh37.p13 chr2: 228,845,946-228,845,946 SPHKAP, LOC105373918
    nsv5613119insertion1nstd207human GRCh38 chr2: 228,142,261-228,142,261 , GRCh37.p13 chr2: 229,006,977-229,006,977 SPHKAP
    nsv5605420insertion1nstd207human GRCh38 chr2: 228,139,910-228,139,910 , GRCh37.p13 chr2: 229,004,626-229,004,626 SPHKAP
    nsv5577334copy number variation1nstd207human GRCh38 chr2: 228,092,251-228,092,310 , GRCh37.p13 chr2: 228,956,967-228,957,026 SPHKAP
    nsv5576318copy number variation1nstd207human GRCh38 chr2: 228,092,432-228,092,506 , GRCh37.p13 chr2: 228,957,148-228,957,222 SPHKAP
    nsv5561051sequence alteration1nstd206human GRCh38 chr2: 227,980,232-227,980,237 , GRCh37.p13 chr2: 228,844,948-228,844,953 SPHKAP, LOC105373918
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5553902insertion1nstd206human GRCh38 chr2: 227,980,232-227,980,232 , GRCh37.p13 chr2: 228,844,948-228,844,948 SPHKAP, LOC105373918
    nsv5452875copy number variation1nstd206human GRCh38 chr2: 228,053,759-228,060,437 , GRCh37.p13 chr2: 228,918,475-228,925,153 SPHKAP
    nsv5449552copy number variation1nstd206human GRCh38 chr2: 228,120,156-228,124,614 , GRCh37.p13 chr2: 228,984,872-228,989,330 SPHKAP
    nsv5445532copy number variation1nstd206human GRCh38 chr2: 228,043,944-228,049,882 , GRCh37.p13 chr2: 228,908,660-228,914,598 SPHKAP
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