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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973065inversion1nstd209human GRCh38 chr4: 87,164,994-87,871,049 , GRCh37.p13 chr4: 88,086,146-88,792,201 DMP1, DSPP, 16 more genes
    nsv5907258copy number variation1nstd209human GRCh38 chr4: 87,165,110-92,683,258 , GRCh37.p13 chr4: 88,086,262-93,604,409 HSP90AB3P, SPP1, 61 more genes
    nsv5691965mobile element insertion2nstd211human GRCh38 chr4: 87,841,456-87,841,456 , GRCh37.p13 chr4: 88,762,608-88,762,608 MEPE
    nsv5572073copy number variation1nstd207human GRCh38 chr4: 87,829,743-87,829,822 , GRCh37.p13 chr4: 88,750,895-88,750,974 MEPE
    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
    nsv5464213copy number variation1nstd206human GRCh38 chr4: 87,829,751-87,829,823 , GRCh37.p13 chr4: 88,750,903-88,750,975 MEPE
    nsv5407369mobile element insertion1nstd206human GRCh38 chr4: 87,841,456-87,841,507 , GRCh37.p13 chr4: 88,762,608-88,762,659 MEPE
    nsv5040446inversion1nstd200human GRCh38 chr4: 76,223,829-89,968,114 , GRCh37.p13 chr4: 77,144,982-90,889,265 , KPNA2P1, 209 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4923448copy number variation1nstd200human GRCh38 chr4: 87,772,399-87,847,333 , GRCh37.p13 chr4: 88,693,551-88,768,485 IBSP, MEPE, 1 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
    nsv4702618copy number variation1nstd195human GRCh37 chr4: 88,719,401-88,843,001 , GRCh38.p12 chr4: 87,798,249-87,921,849 HSP90AB3P, IBSP, 1 more genes
    nsv4685891copy number variation1nstd102humanPathogenic GRCh37 chr4: 88,075,149-90,714,489 , GRCh38.p12 chr4: 87,153,997-89,793,338 LOC100419572, HSD17B13, 50 more genes
    nsv4560845mobile element insertion1nstd166human GRCh37.p13 chr4: 88,760,701-88,760,701 , GRCh38.p12 chr4: 87,839,549-87,839,549 MEPE
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