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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 LOC105377327, LOC105377324, 214 more genes
    nsv7096482copy number variation1nstd102humanPathogenic GRCh37 chr4: 100,239,320-100,528,137 , GRCh38.p12 chr4: 99,318,163-99,606,980 ADH1B, ADH1C, 5 more genes
    nsv7054609inversion1nstd229human GRCh38 chr4: 95,257,712-104,152,159 , GRCh37.p13 chr4: 96,178,863-105,073,316 SLC39A8, PABPC1P7, 96 more genes
    nsv7052845inversion1nstd229human GRCh38 chr4: 97,450,222-102,053,198 , GRCh37.p13 chr4: 98,371,373-102,974,355 RNU6-462P, LOC105377345, 58 more genes
    nsv7052661inversion1nstd229human GRCh38 chr4: 96,912,053-103,991,076 , GRCh37.p13 chr4: 97,833,204-104,912,233 MIR1255A, LOC107986297, 86 more genes
    nsv7046928inversion1nstd229human GRCh38 chr4: 95,051,434-103,882,549 , GRCh37.p13 chr4: 95,972,585-104,803,706 PABPC1P7, RN7SL728P, 95 more genes
    nsv7044544inversion1nstd229human GRCh38 chr4: 98,964,941-108,185,877 , GRCh37.p13 chr4: 99,886,092-109,107,033 LOC102725220, TACR3, 117 more genes
    nsv6755080copy number variation1nstd229human GRCh38 chr4: 99,402,184-99,426,169 , GRCh37.p13 chr4: 100,323,341-100,347,326 LOC102723576, ADH7
    nsv6748823copy number variation1nstd229human GRCh38 chr4: 99,420,901-99,422,600 , GRCh37.p13 chr4: 100,342,058-100,343,757 ADH7
    nsv6748722copy number variation1nstd229human GRCh38 chr4: 99,402,129-99,452,942 , GRCh37.p13 chr4: 100,323,286-100,374,099 LOC102723576, ADH7
    nsv6748624copy number variation1nstd229human GRCh38 chr4: 99,414,801-99,470,000 , GRCh37.p13 chr4: 100,335,958-100,391,157 ADH7
    nsv6748119copy number variation1nstd229human GRCh38 chr4: 99,371,675-99,445,512 , GRCh37.p13 chr4: 100,292,832-100,366,669 LOC102723576, ADH7
    nsv6630192copy number variation1nstd224human GRCh37 chr4: 99,863,585-100,335,586 , GRCh38.p12 chr4: 98,942,434-99,414,429 ADH1B, ADH5, 15 more genes
    nsv6389301copy number variation1nstd223human GRCh38 chr4: 99,434,050-99,434,520 , GRCh37.p13 chr4: 100,355,207-100,355,677 ADH7
    nsv6387210copy number variation1nstd223human GRCh38 chr4: 99,402,129-99,452,942 , GRCh37.p13 chr4: 100,323,286-100,374,099 LOC102723576, ADH7
    nsv6378078copy number variation1nstd223human GRCh38 chr4: 99,417,591-99,419,855 , GRCh37.p13 chr4: 100,338,748-100,341,012 ADH7
    nsv6376737copy number variation1nstd223human GRCh38 chr4: 99,180,425-99,444,855 , GRCh37.p13 chr4: 100,101,582-100,366,012 ADH7, LOC100507053, 5 more genes
    nsv6311812copy number variation1nstd102humanUncertain significance GRCh37 chr4: 100,239,320-100,544,005 , GRCh38.p12 chr4: 99,318,163-99,622,848 C4orf17, ADH1B, 5 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
    nsv6291428copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 95,490,755-109,977,216 , GRCh38.p12 chr4: 94,569,604-109,056,060 ADH1A, ADH1B, 157 more genes
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