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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3875513copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,433,876-177,441,189 , GRCh38.p12 chr5: 176,006,873-178,014,188 RAB24, RN7SL684P, 64 more genes
    nsv3875235copy number variation2nstd102humanPathogenic GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788 SPEF2, NDST1, 2490 more genes
    nsv3874802copy number variation1nstd102humanPathogenic GRCh37 chr5: 172,031,248-180,719,789 , GRCh38.p12 chr5: 172,604,245-181,292,788 LINC01863, TBC1D9B, 257 more genes
    nsv3874238copy number variation1nstd102humanPathogenic GRCh37 chr5: 106,716,357-180,687,338 , GRCh38.p12 chr5: 107,380,656-181,260,337 PJA2, LOC646058, 1228 more genes
    nsv3873295copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,570,677-180,719,789 , GRCh38.p12 chr5: 176,143,674-181,292,788 LINC02222, LOC100288803, 186 more genes
    nsv3871533copy number variation1nstd102humanPathogenic GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343 PCDHGC5, RGS14, 2492 more genes
    nsv3871095copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,722,788-177,423,091 , GRCh38.p12 chr5: 176,295,785-177,996,090 PRR7-AS1, MIR1271, 55 more genes
    nsv3538746insertion1nstd152human GRCh38 chr5: 177,096,905-177,096,905 , GRCh37.p13 chr5: 176,523,906-176,523,906 FGFR4
    nsv3537214insertion1nstd152human GRCh38 chr5: 177,097,086-177,097,086 , GRCh37.p13 chr5: 176,524,087-176,524,087 FGFR4
    nsv3536930insertion1nstd152human GRCh38 chr5: 177,097,080-177,097,080 , GRCh37.p13 chr5: 176,524,081-176,524,081 FGFR4
    nsv3536096insertion1nstd152human GRCh38 chr5: 177,097,065-177,097,065 , GRCh37.p13 chr5: 176,524,066-176,524,066 FGFR4
    nsv3535450insertion1nstd152human GRCh38 chr5: 177,097,093-177,097,093 , GRCh37.p13 chr5: 176,524,094-176,524,094 FGFR4
    nsv3534998insertion1nstd152human GRCh38 chr5: 177,097,016-177,097,016 , GRCh37.p13 chr5: 176,524,017-176,524,017 FGFR4
    nsv3398827insertion3nstd162human GRCh38 chr5: 177,096,926-177,096,926 , GRCh37.p13 chr5: 176,523,927-176,523,927 FGFR4
    nsv3397763insertion5nstd162human GRCh38 chr5: 177,097,110-177,097,110 , GRCh37.p13 chr5: 176,524,111-176,524,111 FGFR4
    nsv3397531insertion9nstd162human GRCh38 chr5: 177,096,983-177,096,983 , GRCh37.p13 chr5: 176,523,984-176,523,984 FGFR4
    nsv3392511insertion5nstd162human GRCh38 chr5: 177,097,066-177,097,066 , GRCh37.p13 chr5: 176,524,067-176,524,067 FGFR4
    nsv3389355insertion2nstd162human GRCh38 chr5: 177,096,888-177,096,888 , GRCh37.p13 chr5: 176,523,889-176,523,889 FGFR4
    nsv3379187insertion9nstd162human GRCh38 chr5: 177,096,953-177,096,953 , GRCh37.p13 chr5: 176,523,954-176,523,954 FGFR4
    nsv3199701copy number variation1nstd152human GRCh38 chr5: 177,097,025-177,097,109 , GRCh37.p13 chr5: 176,524,026-176,524,110 FGFR4
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