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Items: 1 to 20 of 143

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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
    nsv5902244copy number variation1nstd209human GRCh38 chr4: 156,014,074-164,864,480 , GRCh37.p13 chr4: 156,935,226-165,785,632 , MIR3688-1, 67 more genes
    nsv5683376mobile element insertion2nstd211human GRCh38 chr4: 157,573,204-157,573,204 , GRCh37.p13 chr4: 158,494,356-158,494,356 LINC02433
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5381776copy number variation1nstd102humanPathogenic GRCh37 chr4: 157,771,352-172,496,278 , GRCh38.p12 chr4: 156,850,200-171,575,127 LOC107986326, LOC107986240, 144 more genes
    nsv5221035copy number variation1nstd204human GRCh38.p13 chr4: 157,575,417-157,576,516 , GRCh37.p13 chr4: 158,496,569-158,497,668 LINC02433
    nsv5097591mobile element insertion1nstd203human GRCh38 chr4: 157,572,968-157,572,984 , GRCh37.p13 chr4: 158,494,120-158,494,136 LINC02433
    nsv5092117mobile element insertion1nstd203human GRCh38 chr4: 157,573,190-157,573,204 , GRCh37.p13 chr4: 158,494,342-158,494,356 LINC02433
    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
    nsv4590135copy number variation1nstd183human GRCh37 chr4: 157,959,931-158,764,202 , GRCh38.p12 chr4: 157,038,779-157,843,050 , GLRB, 6 more genes
    nsv4474490mobile element insertion1nstd166human GRCh37.p13 chr4: 158,494,342-158,494,342 , GRCh38.p12 chr4: 157,573,190-157,573,190 LINC02433
    nsv4457244copy number variation1nstd102humanPathogenic GRCh37 chr4: 151,174,061-190,957,473 , GRCh38.p12 chr4: 150,252,909-190,036,318 LOC105377509, MIR3140, 487 more genes
    nsv4457215copy number variation1nstd102humanUncertain significance GRCh37 chr4: 158,177,478-163,328,854 , GRCh38.p12 chr4: 157,256,326-162,407,702 LOC105377509, LOC107986239, 36 more genes
    nsv4456414copy number variation1nstd102humanUncertain significance GRCh37 chr4: 154,907,679-159,012,980 , GRCh38.p12 chr4: 153,986,527-158,091,828 LOC105377508, MAP9-AS1, 59 more genes
    nsv4455301copy number variation1nstd102humanPathogenic GRCh37 chr4: 124,873,497-185,278,662 , GRCh38.p12 chr4: 123,952,342-184,357,509 SMARCA5, SFRP2, 633 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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