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Items: 1 to 20 of 258

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5686511mobile element insertion2nstd211human GRCh38 chr4: 139,538,710-139,538,710 , GRCh37.p13 chr4: 140,459,864-140,459,864 SETD7
    nsv5606014insertion1nstd207human GRCh38 chr4: 139,538,697-139,538,697 , GRCh37.p13 chr4: 140,459,851-140,459,851 SETD7
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5558253sequence alteration1nstd206human GRCh38 chr4: 120,373,769-143,797,136 , GRCh37.p13 chr4: 121,294,924-144,718,289 , IL15, 218 more genes
    nsv5556921sequence alteration1nstd206human GRCh38 chr4: 139,551,642-139,551,642 , GRCh37.p13 chr4: 140,472,796-140,472,796 SETD7
    nsv5545226insertion1nstd206human GRCh38 chr4: 139,551,640-139,551,640 , GRCh37.p13 chr4: 140,472,794-140,472,794 SETD7
    nsv5469838copy number variation1nstd206human GRCh38 chr4: 139,500,180-139,500,257 , GRCh37.p13 chr4: 140,421,334-140,421,411 SETD7
    nsv5367863translocation1nstd200human GRCh38 chr15: 50,149,534-50,149,534 , GRCh38 chr4: 139,551,641-139,551,641 , GRCh37.p13 chr15: 50,441,731-50,441,731 , GRCh37.p13 chr4: 140,472,795-140,472,795 SETD7, ATP8B4
    nsv5343770translocation1nstd200human GRCh37 chr15: 50,441,731-50,441,731 , GRCh37 chr4: 140,472,795-140,472,795 , GRCh38.p12 chr15: 50,149,534-50,149,534 , GRCh38.p12 chr4: 139,551,641-139,551,641 SETD7, ATP8B4
    nsv5324341inversion1nstd204human GRCh37.p13 chr4: 137,941,712-143,237,910 , GRCh38.p13 chr4: 137,020,558-142,316,757 , ELF2, 68 more genes
    nsv5094689mobile element insertion1nstd203human GRCh38 chr4: 139,538,697-139,538,710 , GRCh37.p13 chr4: 140,459,851-140,459,864 SETD7
    nsv4944042copy number variation1nstd200human GRCh38 chr4: 139,536,440-139,536,763 , GRCh37.p13 chr4: 140,457,594-140,457,917 SETD7
    nsv4873391inversion1nstd200human GRCh37 chr4: 137,941,721-143,237,901 , GRCh38.p12 chr4: 137,020,567-142,316,748 , MAML3, 68 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
    nsv4746019copy number variation1nstd199human GRCh37 chr4: 140,418,458-140,418,522 , GRCh38.p12 chr4: 139,497,304-139,497,368 SETD7
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