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Items: 1 to 20 of 171

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6754403copy number variation1nstd229human GRCh38 chr4: 164,575,401-164,619,100 , GRCh37.p13 chr4: 165,496,553-165,540,252 RNU6-284P
    nsv6754297copy number variation1nstd229human GRCh38 chr4: 164,584,468-164,988,469 , GRCh37.p13 chr4: 165,505,620-165,909,621 NACA3P, RNU6-284P, 11 more genes
    nsv6753698copy number variation1nstd229human GRCh38 chr4: 164,571,201-164,694,200 , GRCh37.p13 chr4: 165,492,353-165,615,352 RNU6-284P
    nsv6751864copy number variation1nstd229human GRCh38 chr4: 164,039,828-165,202,299 , GRCh37.p13 chr4: 164,960,980-166,123,451 LOC391711, TRIM75, 21 more genes
    nsv6749938copy number variation1nstd229human GRCh38 chr4: 164,620,456-164,623,556 , GRCh37.p13 chr4: 165,541,608-165,544,708 RNU6-284P
    nsv6746282copy number variation1nstd229human GRCh38 chr4: 164,150,106-164,641,964 , GRCh37.p13 chr4: 165,071,258-165,563,116 RNU6-284P, MARCHF1, 2 more genes
    nsv6745645copy number variation1nstd229human GRCh38 chr4: 164,337,602-164,707,336 , GRCh37.p13 chr4: 165,258,754-165,628,488 RNU6-284P, MARCHF1
    nsv6740482copy number variation1nstd229human GRCh38 chr4: 164,057,383-165,303,005 , GRCh37.p13 chr4: 164,978,535-166,224,157 TRIM60P14, LOC391711, 24 more genes
    nsv6636318copy number variation1nstd102humanUncertain significance GRCh37 chr4: 161,461,677-166,911,259 , GRCh38.p12 chr4: 160,540,525-165,990,107 LOC107986325, NACA3P, 60 more genes
    nsv6636305copy number variation1nstd102humanUncertain significance GRCh37 chr4: 165,149,918-165,787,022 , GRCh38.p12 chr4: 164,228,766-164,865,870 MARCHF1, SMIM31, 3 more genes
    nsv6636254copy number variation1nstd102humanUncertain significance GRCh37 chr4: 164,980,534-166,223,066 , GRCh38.p12 chr4: 164,059,382-165,301,914 ANP32CP, GK3, 24 more genes
    nsv6634351copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318 COPS3P1, LOC339975, 363 more genes
    nsv6393456copy number variation1nstd223human GRCh38 chr4: 164,584,468-164,988,469 , GRCh37.p13 chr4: 165,505,620-165,909,621 LOC391710, APELA, 11 more genes
    nsv6391081copy number variation1nstd223human GRCh38 chr4: 164,543,299-164,814,465 , GRCh37.p13 chr4: 165,464,451-165,735,617 SMIM31, CHORDC1P3, 2 more genes
    nsv6313729copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,755,174-190,225,765 , GRCh38.p12 chr4: 158,834,022-189,304,611 NAF1, LOC107986200, 336 more genes
    nsv6134917copy number variation1nstd213human GRCh37 chr4: 163,890,000-165,780,001 , GRCh38.p12 chr4: 162,968,848-164,858,849 NPY1R, NPY5R, 18 more genes
    nsv6134911copy number variation1nstd213human GRCh37 chr4: 147,270,000-190,610,001 , GRCh38.p12 chr4: 146,348,848-189,688,847 , AGA, 517 more genes
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5996239copy number variation1nstd212human GRCh38 chr4: 164,330,115-165,027,122 , GRCh37.p13 chr4: 165,251,267-165,948,274 RPL26P16, TRIM60P14, 16 more genes
    nsv5995781copy number variation1nstd212human GRCh38 chr4: 164,619,135-164,619,207 , GRCh37.p13 chr4: 165,540,287-165,540,359 RNU6-284P
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