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Items: 1 to 20 of 241

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7042720inversion1nstd229human GRCh38 chr4: 157,613,092-158,216,964 , GRCh37.p13 chr4: 158,534,244-159,138,116 NUDT19P5, TMEM144, 5 more genes
    nsv7040627inversion1nstd229human GRCh38 chr4: 158,129,580-158,293,330 , GRCh37.p13 chr4: 159,050,732-159,214,482 TMEM144, GASK1B-AS1, 4 more genes
    nsv6750119copy number variation1nstd229human GRCh38 chr4: 158,227,055-158,241,175 , GRCh37.p13 chr4: 159,148,207-159,162,327 TMEM144
    nsv6745314copy number variation1nstd229human GRCh38 chr4: 158,177,566-158,204,365 , GRCh37.p13 chr4: 159,098,718-159,125,517 NUDT19P5, TMEM144, 2 more genes
    nsv6740368copy number variation1nstd229human GRCh38 chr4: 158,178,301-158,277,600 , GRCh37.p13 chr4: 159,099,453-159,198,752 AIDAP2, GASK1B-AS1, 3 more genes
    nsv6636412copy number variation1nstd102humanUncertain significance GRCh37 chr4: 158,682,606-159,762,612 , GRCh38.p12 chr4: 157,761,454-158,841,460 LOC105377509, GASK1B, 15 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
    nsv6569491inversion1nstd223human GRCh38 chr4: 158,248,223-158,249,214 , GRCh37.p13 chr4: 159,169,375-159,170,366 TMEM144
    nsv6393504copy number variation1nstd223human GRCh38 chr4: 158,240,825-158,241,357 , GRCh37.p13 chr4: 159,161,977-159,162,509 TMEM144
    nsv6388526copy number variation1nstd223human GRCh38 chr4: 158,223,675-158,224,198 , GRCh37.p13 chr4: 159,144,827-159,145,350 TMEM144
    nsv6387157copy number variation1nstd223human GRCh38 chr4: 158,251,284-158,251,763 , GRCh37.p13 chr4: 159,172,436-159,172,915 TMEM144
    nsv6381993copy number variation1nstd223human GRCh38 chr4: 158,251,244-158,256,828 , GRCh37.p13 chr4: 159,172,396-159,177,980 TMEM144
    nsv6378794copy number variation1nstd223human GRCh38 chr4: 158,049,342-158,252,026 , GRCh37.p13 chr4: 158,970,494-159,173,178 GASK1B, LOC105377509, 4 more genes
    nsv6290701copy number variation1nstd102humanUncertain significance GRCh37 chr4: 159,101,199-159,197,057 , GRCh38.p12 chr4: 158,180,047-158,275,905 TMEM144, LOC101928007, 3 more genes
    nsv6135302copy number variation1nstd213human GRCh37 chr4: 159,070,000-159,260,001 , GRCh38.p12 chr4: 158,148,848-158,338,849 GASK1B, TMEM144, 4 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
    nsv6134884copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,720,001 , GRCh38.p12 chr4: 108,308,844-160,798,849 , ANK2, 616 more genes
    nsv6134731copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,710,001 , GRCh38.p12 chr4: 108,308,844-160,788,849 , ANK2, 616 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
    nsv5902244copy number variation1nstd209human GRCh38 chr4: 156,014,074-164,864,480 , GRCh37.p13 chr4: 156,935,226-165,785,632 , MIR3688-1, 67 more genes
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