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Items: 1 to 20 of 125

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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
    nsv5463768copy number variation1nstd206human GRCh38 chr4: 116,048,225-116,785,496 , GRCh37.p13 chr4: 116,969,381-117,706,652 LOC105377385, TRMT112P1, 9 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
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 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
    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
    nsv4596807copy number variation1nstd183human GRCh37 chr4: 116,850,887-117,769,823 , GRCh38.p12 chr4: 115,929,731-116,848,667 TRMT112P1, RLFP1, 11 more genes
    nsv4589663copy number variation1nstd183human GRCh37 chr4: 117,511,705-117,533,052 , GRCh38.p12 chr4: 116,590,549-116,611,896 ACTN4P1
    nsv4587252copy number variation1nstd183human GRCh37 chr4: 116,855,196-117,778,168 , GRCh38.p12 chr4: 115,934,040-116,857,012 MTRNR2L13, LOC105377383, 12 more genes
    nsv4587169copy number variation1nstd183human GRCh37 chr4: 117,500,538-117,518,398 , GRCh38.p12 chr4: 116,579,382-116,597,242 ACTN4P1
    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
    nsv4393988copy number variation1nstd174human GRCh37 chr4: 117,074,400-118,178,149 , GRCh38.p12 chr4: 116,153,244-117,256,993 TRAM1L1, CUL4AP1, 13 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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