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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7097256copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr4: 55,124,936-57,368,027 , GRCh38.p12 chr4: 54,258,769-56,501,861 AASDH, EXOC1, 40 more genes
    nsv7042838inversion1nstd229human GRCh38 chr4: 55,519,343-61,509,140 , GRCh37.p13 chr4: 56,385,510-62,374,858 LINC02271, CHAER1, 59 more genes
    nsv6735924copy number variation1nstd229human GRCh38 chr4: 55,830,194-55,830,304 , GRCh37.p13 chr4: 56,696,360-56,696,470 EXOC1L
    nsv6732261copy number variation1nstd229human GRCh38 chr4: 55,692,600-55,954,831 , GRCh37.p13 chr4: 56,558,767-56,820,997 EXOC1, RNU6-276P, 5 more genes
    nsv6722401copy number variation1nstd229human GRCh38 chr4: 55,556,580-55,828,542 , GRCh37.p13 chr4: 56,422,747-56,694,708 EXOC1L, LOC105377661, 4 more genes
    nsv6720279copy number variation1nstd229human GRCh38 chr4: 55,564,862-55,964,774 , GRCh37.p13 chr4: 56,431,029-56,830,940 EXOC1, NMU, 8 more genes
    nsv6637063copy number variation1nstd102humanUncertain significance GRCh37 chr4: 52,685,980-59,272,025 , GRCh38.p12 chr4: 51,819,814-58,405,859 SPINK2, RN7SL492P, 100 more genes
    nsv6395116copy number variation1nstd223human GRCh38 chr4: 55,828,043-55,828,721 , GRCh37.p13 chr4: 56,694,209-56,694,887 EXOC1L
    nsv6392591copy number variation1nstd223human GRCh38 chr4: 55,834,414-55,835,076 , GRCh37.p13 chr4: 56,700,580-56,701,242 EXOC1L
    nsv6311837copy number variation2nstd102humanUncertain significance GRCh37 chr4: 55,124,936-57,798,318 , GRCh38.p12 chr4: 54,258,769-56,932,152 GLDCP1, KDR, 54 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6291206copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,685,685-58,104,722 , GRCh38.p12 chr4: 51,819,519-57,238,556 SRD5A3, DCUN1D4, 96 more genes
    nsv6291075copy number variation1nstd102humanLikely benign GRCh37 chr4: 56,531,648-56,784,257 , GRCh38.p12 chr4: 55,665,481-55,918,091 EXOC1, EXOC1L, 4 more genes
    nsv6135345copy number variation1nstd213human GRCh37 chr4: 55,360,000-63,180,001 , GRCh38.p12 chr4: 54,493,833-62,314,283 GLDCP1, IGFBP7, 82 more genes
    nsv6134939copy number variation1nstd213human GRCh37 chr4: 55,330,000-63,180,001 , GRCh38.p12 chr4: 54,463,833-62,314,283 GLDCP1, IGFBP7, 82 more genes
    nsv5904688copy number variation1nstd209human GRCh38 chr4: 55,818,953-55,823,186 , GRCh37.p13 chr4: 56,685,119-56,689,352 LOC105377661, EXOC1L
    nsv5687808mobile element insertion1nstd211human GRCh38 chr4: 55,835,336-55,835,336 , GRCh37.p13 chr4: 56,701,502-56,701,502 EXOC1L
    nsv5686089mobile element insertion2nstd211human GRCh38 chr4: 55,830,632-55,830,632 , GRCh37.p13 chr4: 56,696,798-56,696,798 EXOC1L
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
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