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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969033inversion1nstd209human GRCh38 chr4: 108,267,752-117,667,772 , GRCh37.p13 chr4: 109,188,908-118,588,927 , ANK2, 134 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5471174copy number variation1nstd206human GRCh38 chr4: 109,700,748-109,700,843 , GRCh37.p13 chr4: 110,621,904-110,621,999 CASP6
    nsv5367751translocation1nstd200human GRCh38 chr4: 109,697,619-109,697,619 , GRCh38 chr4: 109,694,700-109,694,700 , GRCh37.p13 chr4: 110,618,775-110,618,775 , GRCh37.p13 chr4: 110,615,856-110,615,856 CASP6
    nsv5367749translocation1nstd200human GRCh38 chr4: 109,689,569-109,689,569 , GRCh38 chr4: 109,694,523-109,694,523 , GRCh37.p13 chr4: 110,615,679-110,615,679 , GRCh37.p13 chr4: 110,610,725-110,610,725 CASP6
    nsv5346974translocation1nstd200human GRCh38 chr4: 109,691,011-109,691,011 , GRCh38 chr4: 109,694,523-109,694,523 , GRCh37.p13 chr4: 110,612,167-110,612,167 , GRCh37.p13 chr4: 110,615,679-110,615,679 CASP6
    nsv5346973translocation1nstd200human GRCh38 chr4: 109,690,848-109,690,848 , GRCh38 chr4: 109,689,570-109,689,570 , GRCh37.p13 chr4: 110,610,726-110,610,726 , GRCh37.p13 chr4: 110,612,004-110,612,004 CASP6
    nsv5215577mobile element deletion1nstd204human GRCh38.p13 chr4: 109,702,319-109,702,621 , GRCh37.p13 chr4: 110,623,475-110,623,777 CASP6
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4883100mobile element deletion1nstd200human GRCh38 chr4: 109,702,325-109,702,615 , GRCh37.p13 chr4: 110,623,481-110,623,771 CASP6
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4778131mobile element deletion1nstd200human GRCh37 chr4: 110,623,481-110,623,771 , GRCh38.p12 chr4: 109,702,325-109,702,615 CASP6
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4455413copy number variation1nstd102humanUncertain significance GRCh37 chr4: 110,386,827-110,660,498 , GRCh38.p12 chr4: 109,465,671-109,739,342 CASP6, SETP20, 7 more genes
    nsv4342697sequence alteration1nstd166human GRCh37.p13 chr4: 73,901,505-160,870,682 , GRCh38.p12 chr4: 73,035,788-159,949,530 , ADH1B, 1083 more genes
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