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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5873481copy number variation1nstd209human GRCh38 chr1: 153,419,111-153,428,488 , GRCh37.p13 chr1: 153,391,587-153,400,964 S100A8, S100A7P1, 1 more genes
    nsv5828145copy number variation1nstd209human GRCh38 chr1: 153,419,076-153,421,410 , GRCh37.p13 chr1: 153,391,552-153,393,886 S100A8, S100A7A
    nsv5563935sequence alteration1nstd206human GRCh38 chr1: 153,417,880-153,459,217 , GRCh37.p13 chr1: 153,390,356-153,431,693 S100A7, S100A8, 4 more genes
    nsv5556873inversion1nstd206human GRCh38 chr1: 153,417,393-153,459,649 , GRCh37.p13 chr1: 153,389,869-153,432,125 S100A7, S100A8, 4 more genes
    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
    nsv5331063translocation1nstd200human GRCh37 chr1: 153,431,452-153,431,452 , GRCh37 chr1: 153,390,590-153,390,590 , GRCh38.p12 chr1: 153,418,114-153,418,114 , GRCh38.p12 chr1: 153,458,976-153,458,976 S100A7, S100A8, 1 more genes
    nsv4903888copy number variation1nstd200human GRCh38 chr1: 153,340,507-153,523,038 , GRCh37.p13 chr1: 153,312,983-153,495,514 S100A8, S100A7P1, 10 more genes
    nsv4897450copy number variation1nstd200human GRCh38 chr1: 153,418,888-153,419,652 , GRCh37.p13 chr1: 153,391,364-153,392,128 S100A7A, S100A8
    nsv4781202copy number variation1nstd200human GRCh37 chr1: 153,312,983-153,495,514 , GRCh38.p12 chr1: 153,340,507-153,523,038 S100A9, S100A12, 10 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
    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
    nsv4708254copy number variation1nstd195human GRCh37 chr1: 153,385,351-153,414,501 , GRCh38.p12 chr1: 153,412,875-153,442,025 S100A8, S100A7P1, 2 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
    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
    nsv3902729copy number variation1nstd102humanUncertain significance NCBI36 chr1: 151,190,269-151,734,755 , GRCh37 chr1: 152,923,645-153,468,131 , GRCh38 chr1: 152,951,169-153,495,655 SPRR3, SPRR2E, 28 more genes
    nsv3900459copy number variation1nstd102humanPathogenic GRCh38 chr1: 149,854,269-180,267,197 , NCBI36 chr1: 148,092,455-178,502,955 , GRCh37 chr1: 149,825,831-180,236,332 HORMAD1, BCAN-AS1, 923 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 , SNAP47, 4927 more genes
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