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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5714640mobile element insertion1nstd211human GRCh38 chr1: 153,535,507-153,535,507 , GRCh37.p13 chr1: 153,507,983-153,507,983 S100A5, S100A6
    nsv5423228copy number variation1nstd206human GRCh38 chr1: 153,535,263-153,535,363 , GRCh37.p13 chr1: 153,507,739-153,507,839 S100A5, S100A6
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv4903889copy number variation1nstd200human GRCh38 chr1: 153,441,299-153,571,038 , GRCh37.p13 chr1: 153,413,775-153,543,514 S100A2, S100A5, 7 more genes
    nsv4897457copy number variation1nstd200human GRCh38 chr1: 153,529,724-153,543,672 , GRCh37.p13 chr1: 153,502,200-153,516,148 S100A6, S100A4, 1 more genes
    nsv4897455copy number variation1nstd200human GRCh38 chr1: 153,520,055-153,539,239 , GRCh37.p13 chr1: 153,492,531-153,511,715 S100A6, S100A5
    nsv4784251copy number variation1nstd200human GRCh37 chr1: 153,492,518-153,511,716 , GRCh38.p12 chr1: 153,520,042-153,539,240 S100A6, S100A5
    nsv4781203copy number variation1nstd200human GRCh37 chr1: 153,413,775-153,543,514 , GRCh38.p12 chr1: 153,441,299-153,571,038 S100A2, S100A5, 7 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4706115copy number variation1nstd195human GRCh38.p12 chr1: 153,454,575-153,574,425 , GRCh37 chr1: 153,427,051-153,546,901 S100A2, S100A3, 6 more genes
    nsv4673972copy number variation1nstd102humanUncertain significance GRCh37 chr1: 153,061,323-153,904,594 , GRCh38.p12 chr1: 153,088,847-153,932,118 S100A15A, LOC343052, 46 more genes
    nsv4451737copy number variation1nstd102humanUncertain significance GRCh37 chr1: 153,321,482-153,835,605 , GRCh38.p12 chr1: 153,349,006-153,863,129 S100A7, NPR1, 33 more genes
    nsv4070119copy number variation1nstd166human GRCh37.p13 chr1: 153,467,507-153,573,590 , GRCh38.p12 chr1: 153,495,031-153,601,114 S100A2, S100A3, 5 more genes
    nsv4059943copy number variation1nstd166human GRCh37.p13 chr1: 153,515,368-153,520,281 , GRCh38.p12 chr1: 153,542,892-153,547,805 S100A3, LOC101928034, 2 more genes
    nsv4054341copy number variation1nstd166human GRCh37.p13 chr1: 153,493,000-153,511,500 , GRCh38.p12 chr1: 153,520,524-153,539,024 S100A6, S100A5
    nsv3962949insertion1nstd168human GRCh38 chr1: 153,515,773-153,537,401 , GRCh37.p13 chr1: 153,488,249-153,509,877 S100A5, S100A6
    nsv3960809inversion1nstd168human GRCh38 chr1: 153,470,551-153,537,401 , GRCh37.p13 chr1: 153,443,027-153,509,877 S100A5, S100A6, 1 more genes
    nsv3918947copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,475,856-247,199,719 , GRCh37.p13 chr1: 145,764,499-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 , LOC101060227, 1608 more genes
    nsv3912840copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 , CRB1, 1608 more genes
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