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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5905664copy number variation1nstd209human GRCh38 chr4: 78,663,182-78,664,428 , GRCh37.p13 chr4: 79,584,336-79,585,582 LINC01094
    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
    nsv5367619translocation1nstd200human GRCh38 chr4: 78,463,095-78,463,095 , GRCh38 chr4: 78,678,686-78,678,686 , GRCh37.p13 chr4: 79,384,249-79,384,249 , GRCh37.p13 chr4: 79,599,840-79,599,840 LINC01094, FRAS1
    nsv5092892mobile element insertion1nstd203human GRCh38 chr4: 78,644,571-78,644,588 , GRCh37.p13 chr4: 79,565,725-79,565,742 LINC01094
    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
    nsv5032677inversion1nstd200human GRCh38 chr4: 74,153,605-79,796,520 , GRCh37.p13 chr4: 75,019,322-80,717,674 , LINC01094, 104 more genes
    nsv4925836copy number variation1nstd200human GRCh38 chr4: 78,626,085-78,700,809 , GRCh37.p13 chr4: 79,547,239-79,621,963 LINC01094, HIGD1AP13
    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
    nsv4680308copy number variation1nstd189human GRCh37.p13 chr4: 79,256,941-79,576,494 , GRCh38.p12 chr4: 78,335,787-78,655,340 ANXA3, FRAS1, 3 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
    nsv4674141copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,950,363-79,738,598 , GRCh38.p12 chr4: 68,084,645-78,817,444 COX18, UGT2B11, 216 more genes
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