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Items: 1 to 20 of 291

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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
    nsv5979034inversion1nstd209human GRCh38 chr4: 136,299,558-138,570,240 , GRCh37.p13 chr4: 137,220,713-139,491,394 SLC7A11, PCDH18, 20 more genes
    nsv5900342copy number variation1nstd209human GRCh38 chr4: 138,177,680-138,177,760 , GRCh37.p13 chr4: 139,098,834-139,098,914 SLC7A11, SLC7A11-AS1
    nsv5717063mobile element insertion1nstd211human GRCh38 chr4: 138,187,670-138,187,670 , GRCh37.p13 chr4: 139,108,824-139,108,824 SLC7A11
    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
    nsv5549976insertion1nstd206human GRCh38 chr4: 138,191,008-138,191,059 , GRCh37.p13 chr4: 139,112,162-139,112,213 SLC7A11
    nsv5324341inversion1nstd204human GRCh37.p13 chr4: 137,941,712-143,237,910 , GRCh38.p13 chr4: 137,020,558-142,316,757 , ELF2, 68 more genes
    nsv5088699mobile element insertion1nstd203human GRCh38 chr4: 138,192,028-138,192,039 , GRCh37.p13 chr4: 139,113,182-139,113,193 SLC7A11
    nsv4945941copy number variation1nstd200human GRCh38 chr4: 138,228,736-138,240,536 , GRCh37.p13 chr4: 139,149,890-139,161,690 SLC7A11
    nsv4945940copy number variation1nstd200human GRCh38 chr4: 138,167,487-138,171,478 , GRCh37.p13 chr4: 139,088,641-139,092,632 SLC7A11-AS1, SLC7A11
    nsv4945939copy number variation1nstd200human GRCh38 chr4: 138,167,077-138,170,323 , GRCh37.p13 chr4: 139,088,231-139,091,477 SLC7A11, SLC7A11-AS1
    nsv4945930copy number variation1nstd200human GRCh38 chr4: 137,835,401-138,666,632 , GRCh37.p13 chr4: 138,756,555-139,587,786 SLC7A11, LOC152594, 7 more genes
    nsv4873391inversion1nstd200human GRCh37 chr4: 137,941,721-143,237,901 , GRCh38.p12 chr4: 137,020,567-142,316,748 , MAML3, 68 more genes
    nsv4792409copy number variation1nstd200human GRCh37 chr4: 139,088,231-139,091,477 , GRCh38.p12 chr4: 138,167,077-138,170,323 SLC7A11-AS1, SLC7A11
    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
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