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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5553170insertion1nstd206human GRCh38 chr1: 153,118,273-153,118,305 , GRCh37.p13 chr1: 153,090,749-153,090,781 SPRR2F
    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
    nsv5287542copy number variation1nstd204human GRCh38.p13 chr1: 153,096,026-153,115,848 , GRCh37.p13 chr1: 153,068,502-153,088,324 SPRR2F
    nsv5206684copy number variation1nstd204human GRCh38.p13 chr1: 153,096,512-153,113,885 , GRCh37.p13 chr1: 153,068,988-153,086,361 SPRR2F
    nsv5203099copy number variation1nstd204human GRCh38.p13 chr1: 153,115,901-153,119,900 , GRCh37.p13 chr1: 153,088,377-153,092,376 SPRR2F
    nsv5202025copy number variation1nstd204human GRCh38.p13 chr1: 153,116,201-153,118,300 , GRCh37.p13 chr1: 153,088,677-153,090,776 SPRR2F
    nsv4903885copy number variation1nstd200human GRCh38 chr1: 153,112,422-153,140,608 , GRCh37.p13 chr1: 153,084,898-153,113,084 SPRR2C, SPRR2F
    nsv4903884copy number variation1nstd200human GRCh38 chr1: 153,096,378-153,115,492 , GRCh37.p13 chr1: 153,068,854-153,087,968 SPRR2F
    nsv4897432copy number variation1nstd200human GRCh38 chr1: 153,092,982-153,111,903 , GRCh37.p13 chr1: 153,065,458-153,084,379 SPRR2F, SPRR2E
    nsv4781200copy number variation1nstd200human GRCh37 chr1: 153,068,850-153,087,962 , GRCh38.p12 chr1: 153,096,374-153,115,486 SPRR2F
    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
    nsv4728602copy number variation1nstd102humanUncertain significance GRCh37 chr1: 153,007,105-153,463,223 , GRCh38.p12 chr1: 153,034,629-153,490,747 S100A8, S100A7P1, 23 more genes
    nsv4711838copy number variation1nstd195human GRCh37 chr1: 153,083,501-153,115,051 , GRCh38.p12 chr1: 153,111,025-153,142,575 SPRR2C, SPRR2F
    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
    nsv4593965copy number variation2nstd183human GRCh37 chr1: 153,069,195-153,087,963 , GRCh38.p12 chr1: 153,096,719-153,115,487 SPRR2F
    nsv4518402copy number variation1nstd166human GRCh37.p13 chr1: 152,648,171-153,289,950 , GRCh38.p12 chr1: 152,675,695-153,317,474 SPRR2D, SMCP, 36 more genes
    nsv4399666copy number variation1nstd174human GRCh37 chr1: 153,068,826-153,088,338 , GRCh38.p12 chr1: 153,096,350-153,115,862 SPRR2F
    nsv4061733copy number variation1nstd166human GRCh37.p13 chr1: 153,065,553-153,182,302 , GRCh38.p12 chr1: 153,093,077-153,209,826 SPRR2C, SPRR2E, 4 more genes
    nsv4061583copy number variation1nstd166human GRCh37.p13 chr1: 153,068,878-153,087,940 , GRCh38.p12 chr1: 153,096,402-153,115,464 SPRR2F
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