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Items: 1 to 20 of 261

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960529insertion1nstd209human GRCh38 chr4: 174,497,568-174,497,568 , GRCh37.p13 chr4: 175,418,719-175,418,719 HPGD
    nsv5715210mobile element insertion1nstd211human GRCh38 chr4: 174,506,761-174,506,761 , GRCh37.p13 chr4: 175,427,912-175,427,912 HPGD
    nsv5693666mobile element insertion2nstd211human GRCh38 chr4: 174,519,006-174,519,006 , GRCh37.p13 chr4: 175,440,157-175,440,157 HPGD
    nsv5562418mobile element insertion1nstd206human GRCh38 chr4: 174,506,761-174,506,812 , GRCh37.p13 chr4: 175,427,912-175,427,963 HPGD
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5455708copy number variation1nstd206human GRCh38 chr4: 174,496,965-174,511,818 , GRCh37.p13 chr4: 175,418,116-175,432,969 HPGD
    nsv5398126mobile element insertion1nstd206human GRCh38 chr4: 174,519,006-174,519,057 , GRCh37.p13 chr4: 175,440,157-175,440,208 HPGD
    nsv5328644inversion1nstd204human GRCh38.p13 chr4: 174,358,686-174,536,155 , GRCh37.p13 chr4: 175,279,837-175,457,306 HPGD, MIR4276, 2 more genes
    nsv5315801copy number variation1nstd204human GRCh38.p13 chr4: 174,523,283-174,568,054 , GRCh37.p13 chr4: 175,444,434-175,489,205 HPGD, LOC105377548, 1 more genes
    nsv5235183copy number variation1nstd204human GRCh38.p13 chr4: 174,523,034-174,556,804 , GRCh37.p13 chr4: 175,444,185-175,477,955 LOC105377548, HPGD, 1 more genes
    nsv5083669mobile element insertion1nstd203human GRCh38 chr4: 174,519,883-174,519,883 , GRCh37.p13 chr4: 175,441,034-175,441,034 HPGD
    nsv4944062copy number variation1nstd200human GRCh38 chr4: 173,724,041-174,933,391 , GRCh37.p13 chr4: 174,645,192-175,854,542 LOC107986204, LOC101928551, 16 more genes
    nsv4930056copy number variation1nstd200human GRCh38 chr4: 174,496,965-174,511,818 , GRCh37.p13 chr4: 175,418,116-175,432,969 HPGD
    nsv4930055copy number variation1nstd200human GRCh38 chr4: 174,491,468-174,492,766 , GRCh37.p13 chr4: 175,412,619-175,413,917 HPGD
    nsv4871654inversion1nstd200human GRCh37 chr4: 175,279,838-175,457,298 , GRCh38.p12 chr4: 174,358,687-174,536,147 HPGD, MIR4276, 2 more genes
    nsv4801779copy number variation1nstd200human GRCh37 chr4: 175,418,115-175,432,970 , GRCh38.p12 chr4: 174,496,964-174,511,819 HPGD
    nsv4794692copy number variation1nstd200human GRCh37 chr4: 175,444,444-175,489,199 , GRCh38.p12 chr4: 174,523,293-174,568,048 HPGD, LOC100419741, 1 more genes
    nsv4794687copy number variation1nstd200human GRCh37 chr4: 174,645,192-175,854,542 , GRCh38.p12 chr4: 173,724,041-174,933,391 LOC105377547, LINC02269, 16 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
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