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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923455copy number variation1nstd209human GRCh38 chr7: 43,156,668-43,156,731 , GRCh37.p13 chr7: 43,196,267-43,196,330 HECW1, HECW1-IT1
    nsv5920095copy number variation1nstd209human GRCh38 chr7: 43,141,671-43,144,347 , GRCh37.p13 chr7: 43,181,270-43,183,946 HECW1-IT1, HECW1
    nsv5917477copy number variation1nstd209human GRCh38 chr7: 43,129,452-43,129,819 , GRCh37.p13 chr7: 43,169,051-43,169,418 HECW1, HECW1-IT1
    nsv5846607copy number variation1nstd209human GRCh38 chr7: 43,141,741-43,143,840 , GRCh37.p13 chr7: 43,181,340-43,183,439 HECW1, HECW1-IT1
    nsv5584095copy number variation1nstd207human GRCh38 chr7: 43,128,820-43,128,964 , GRCh37.p13 chr7: 43,168,419-43,168,563 HECW1-IT1, HECW1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5481274copy number variation1nstd206human GRCh38 chr7: 43,141,671-43,144,352 , GRCh37.p13 chr7: 43,181,270-43,183,951 HECW1, HECW1-IT1
    nsv5477128copy number variation1nstd206human GRCh38 chr7: 43,129,455-43,129,820 , GRCh37.p13 chr7: 43,169,054-43,169,419 HECW1-IT1, HECW1
    nsv5474436copy number variation1nstd206human GRCh38 chr7: 43,128,820-43,128,965 , GRCh37.p13 chr7: 43,168,419-43,168,564 HECW1, HECW1-IT1
    nsv5381783copy number variation1nstd102humanPathogenic GRCh37 chr7: 41,124,364-47,945,566 , GRCh38.p12 chr7: 41,084,766-47,905,969 ELK1P1, URGCP, 121 more genes
    nsv5378726translocation1nstd200human GRCh38 chr7: 43,129,820-43,129,820 , GRCh38 chr7: 43,129,455-43,129,455 , GRCh37.p13 chr7: 43,169,419-43,169,419 , GRCh37.p13 chr7: 43,169,054-43,169,054 HECW1, HECW1-IT1
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4956385copy number variation1nstd200human GRCh38 chr7: 43,145,049-43,147,303 , GRCh37.p13 chr7: 43,184,648-43,186,902 HECW1, HECW1-IT1
    nsv4956384copy number variation1nstd200human GRCh38 chr7: 43,128,320-43,129,317 , GRCh37.p13 chr7: 43,167,919-43,168,916 HECW1, HECW1-IT1
    nsv4956383copy number variation1nstd200human GRCh38 chr7: 43,118,705-43,120,080 , GRCh37.p13 chr7: 43,158,304-43,159,679 HECW1-IT1, HECW1
    nsv4953626copy number variation1nstd200human GRCh38 chr7: 42,376,110-43,620,617 , GRCh37.p13 chr7: 42,415,709-43,660,216 TCP1P1, LOC105375250, 19 more genes
    nsv4492306mobile element insertion1nstd166human GRCh37.p13 chr7: 43,174,450-43,174,450 , GRCh38.p12 chr7: 43,134,851-43,134,851 HECW1-IT1, HECW1
    nsv4456214copy number variation2nstd102humanUncertain significance GRCh37 chr7: 42,417,642-43,658,492 , GRCh38.p12 chr7: 42,378,043-43,618,893 RPL18AP10, LOC105375252, 19 more genes
    nsv4455566copy number variation1nstd102humanUncertain significance GRCh37 chr7: 42,421,780-43,664,397 , GRCh38.p12 chr7: 42,382,181-43,624,798 RNU7-35P, LINC01448, 19 more genes
    nsv4455279copy number variation1nstd102humanUncertain significance GRCh37 chr7: 40,198,215-43,252,984 , GRCh38.p12 chr7: 40,158,616-43,213,385 INHBA, LOC105375244, 34 more genes
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