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Items: 1 to 20 of 121

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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
    nsv5968674inversion1nstd209human GRCh38 chr4: 116,884,639-117,230,292 , GRCh37.p13 chr4: 117,805,795-118,151,448 TRAM1L1, LOC105377387, 2 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
    nsv5381774copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,833,638-130,232,122 , GRCh38.p12 chr4: 115,912,482-129,310,967 LOC112268469, LOC105377393, 159 more genes
    nsv5309689copy number variation1nstd204human GRCh38.p13 chr4: 117,066,093-117,118,854 , GRCh37.p13 chr4: 117,987,249-118,040,010 LOC105377388, TRAM1L1, 1 more genes
    nsv5223276copy number variation1nstd204human GRCh38.p13 chr4: 117,063,129-117,112,886 , GRCh37.p13 chr4: 117,984,285-118,034,042 LOC105377387, LOC105377388, 1 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv5030758inversion1nstd200human GRCh38 chr4: 116,884,639-117,230,294 , GRCh37.p13 chr4: 117,805,795-118,151,450 TRAM1L1, LOC105377387, 2 more genes
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4876163inversion1nstd200human GRCh37 chr4: 117,805,795-118,151,450 , GRCh38.p12 chr4: 116,884,639-117,230,294 TRAM1L1, LOC105377387, 2 more genes
    nsv4794433copy number variation1nstd200human GRCh37 chr4: 117,987,252-118,040,007 , GRCh38.p12 chr4: 117,066,096-117,118,851 LOC105377387, LOC105377388, 1 more genes
    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
    nsv4680742copy number variation1nstd189human GRCh37.p13 chr4: 117,076,432-118,150,372 , GRCh38.p12 chr4: 116,155,276-117,229,216 TRAM1L1, ACTN4P1, 13 more genes
    nsv4674641copy number variation1nstd102humanLikely benign GRCh37 chr4: 117,624,138-118,017,424 , GRCh38.p12 chr4: 116,702,982-117,096,268 RNU6-119P, TRAM1L1, 4 more genes
    nsv4674598copy number variation1nstd102humanLikely benign GRCh37 chr4: 117,071,980-118,177,853 , GRCh38.p12 chr4: 116,150,824-117,256,697 LOC107986306, HAVCR1P2, 13 more genes
    nsv4436254copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 116,624,547-126,168,646 , GRCh38.p12 chr4: 115,703,391-125,247,491 ANXA5, CCNA2, 125 more genes
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