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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5716824mobile element insertion1nstd211human GRCh38 chr4: 82,128,527-82,128,527 , GRCh37.p13 chr4: 83,049,680-83,049,680 HNRNPA3P13
    nsv5562530mobile element insertion1nstd206human GRCh38 chr4: 82,128,527-82,128,578 , GRCh37.p13 chr4: 83,049,680-83,049,731 HNRNPA3P13
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5161062mobile element insertion1nstd203human GRCh38 chr4: 82,132,076-82,132,092 , GRCh37.p13 chr4: 83,053,229-83,053,245 HNRNPA3P13
    nsv5040446inversion1nstd200human GRCh38 chr4: 76,223,829-89,968,114 , GRCh37.p13 chr4: 77,144,982-90,889,265 , KPNA2P1, 209 more genes
    nsv5037291inversion1nstd200human GRCh38 chr4: 74,160,096-84,998,626 , GRCh37.p13 chr4: 75,025,813-85,919,779 , LOC105377302, 175 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
    nsv4729598copy number variation1nstd102humanPathogenic GRCh37 chr4: 71,412,409-87,920,784 , GRCh38.p12 chr4: 70,546,692-86,999,632 PTPN11P5, LOC643014, 244 more genes
    nsv4674589copy number variation1nstd102humanPathogenic GRCh37 chr4: 72,680,879-86,426,232 , GRCh38.p12 chr4: 71,815,162-85,505,079 SOWAHB, FTLP9, 211 more genes
    nsv4674496copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 83,026,373-83,367,140 , GRCh38.p12 chr4: 82,105,220-82,445,987 HNRNPD, HNRNPDL, 8 more genes
    nsv4674457copy number variation1nstd102humanPathogenic GRCh37 chr4: 82,593,140-85,651,685 , GRCh38.p12 chr4: 81,671,986-84,730,532 RPL7AP26, TMEM150C, 50 more genes
    nsv4457234copy number variation1nstd102humanPathogenic GRCh37 chr4: 78,769,297-84,968,832 , GRCh38.p12 chr4: 77,848,143-84,047,679 OR7E94P, ABRAXAS1, 87 more genes
    nsv4455792copy number variation1nstd102humanPathogenic GRCh37 chr4: 80,199,183-84,074,906 , GRCh38.p12 chr4: 79,278,029-83,153,753 SNORD144, KPNA2P1, 55 more genes
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