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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5468505copy number variation1nstd206human GRCh38 chr4: 99,948,524-99,948,808 , GRCh37.p13 chr4: 100,869,681-100,869,965 H2AZ1-DT, H2AZ1
    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
    nsv4729197copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 94,692,345-101,308,220 , GRCh38.p12 chr4: 93,771,194-100,387,063 ADH1A, ADH1B, 66 more genes
    nsv4589415copy number variation1nstd183human GRCh37 chr4: 100,851,864-100,872,426 , GRCh38.p12 chr4: 99,930,707-99,951,269 H2AZ1, DNAJB14, 1 more genes
    nsv4586948copy number variation1nstd183human GRCh37 chr4: 100,870,803-100,871,423 , GRCh38.p12 chr4: 99,949,646-99,950,266 H2AZ1, H2AZ1-DT
    nsv4410386copy number variation1nstd174human GRCh37 chr4: 100,870,803-100,871,931 , GRCh38.p12 chr4: 99,949,646-99,950,774 H2AZ1, H2AZ1-DT
    nsv4401486copy number variation1nstd174human GRCh37 chr4: 100,869,249-100,872,113 , GRCh38.p12 chr4: 99,948,092-99,950,956 H2AZ1, H2AZ1-DT
    nsv4342697sequence alteration1nstd166human GRCh37.p13 chr4: 73,901,505-160,870,682 , GRCh38.p12 chr4: 73,035,788-159,949,530 , ADH1B, 1083 more genes
    nsv4337628sequence alteration1nstd166human GRCh37.p13 chr4: 95,972,584-105,073,318 , GRCh38.p12 chr4: 95,051,433-104,152,161 , ADH1B, 98 more genes
    nsv3923951copy number variation1nstd102humanUncertain significance NCBI36 chr4: 99,112,516-101,178,305 , GRCh38 chr4: 97,972,342-100,038,125 , GRCh37 chr4: 98,893,493-100,959,282 ADH4, ABT1P1, 39 more genes
    nsv3923759copy number variation1nstd102humanPathogenic NCBI36 chr4: 58,862,002-102,129,682 , GRCh37.p13 chr4: 59,167,245-101,910,659 , GRCh38.p12 chr4: 58,301,079-100,989,502 EREG, EFL1P2, 530 more genes
    nsv3923733copy number variation1nstd102humanPathogenic GRCh38 chr4: 80,427,023-100,855,441 , GRCh37 chr4: 81,348,177-101,776,598 , NCBI36 chr4: 81,567,201-101,995,621 PDLIM5, PRKG2, 215 more genes
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