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Items: 1 to 20 of 282

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096987copy number variation1nstd102humanUncertain significance GRCh37 chr4: 164,050,049-164,069,606 , GRCh38.p12 chr4: 163,128,897-163,148,454 NAF1
    nsv7053525inversion1nstd229human GRCh38 chr4: 162,923,823-163,648,143 , GRCh37.p13 chr4: 163,844,975-164,569,295 TMA16, RPL35AP12, 10 more genes
    nsv7045511inversion1nstd229human GRCh38 chr4: 162,924,092-163,643,522 , GRCh37.p13 chr4: 163,845,244-164,564,674 LOC107986325, MIR4454, 10 more genes
    nsv6751084copy number variation1nstd229human GRCh38 chr4: 163,145,401-163,147,600 , GRCh37.p13 chr4: 164,066,553-164,068,752 NAF1
    nsv6738365copy number variation1nstd229human GRCh38 chr4: 163,167,377-163,178,792 , GRCh37.p13 chr4: 164,088,529-164,099,944 NAF1, LOC105377517
    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
    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
    nsv6388758copy number variation1nstd223human GRCh38 chr4: 163,109,251-163,109,875 , GRCh37.p13 chr4: 164,030,403-164,031,027 NAF1, LOC101928081
    nsv6387755copy number variation1nstd223human GRCh38 chr4: 163,092,479-163,107,527 , GRCh37.p13 chr4: 164,013,631-164,028,679 MIR4454, NAF1
    nsv6386300copy number variation1nstd223human GRCh38 chr4: 161,988,485-163,518,477 , GRCh37.p13 chr4: 162,909,637-164,439,629 LOC105377517, TKTL2, 13 more genes
    nsv6379186copy number variation1nstd223human GRCh38 chr4: 163,111,495-163,112,079 , GRCh37.p13 chr4: 164,032,647-164,033,231 NAF1, LOC101928081
    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
    nsv6255626mobile element insertion1nstd215human GRCh38 chr4: 163,163,640-163,163,640 , GRCh37.p13 chr4: 164,084,792-164,084,792 NAF1
    nsv6255625mobile element insertion1nstd215human GRCh38 chr4: 163,110,342-163,110,342 , GRCh37.p13 chr4: 164,031,494-164,031,494 NAF1, LOC101928081
    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
    nsv6074493insertion1nstd212human GRCh38 chr4: 163,163,625-163,163,625 , GRCh37.p13 chr4: 164,084,777-164,084,777 NAF1
    nsv6061509insertion1nstd212human GRCh38 chr4: 163,110,329-163,110,329 , GRCh37.p13 chr4: 164,031,481-164,031,481 LOC101928081, NAF1
    nsv5995772copy number variation1nstd212human GRCh38 chr4: 163,155,889-163,156,229 , GRCh37.p13 chr4: 164,077,041-164,077,381 NAF1
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