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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5916698copy number variation1nstd209human GRCh38 chr8: 6,923,220-6,923,396 , GRCh37.p13 chr8: 6,780,742-6,780,918 DEFA6
    nsv5907760copy number variation1nstd209human GRCh38 chr8: 6,923,159-6,923,450 , GRCh37.p13 chr8: 6,780,681-6,780,972 DEFA6
    nsv5490620copy number variation1nstd206human GRCh38 chr8: 6,692,000-7,616,000 , GRCh37.p13 chr8: 6,549,521-7,473,522 LOC100422495, DEFT1P, 64 more genes
    nsv5485612copy number variation1nstd206human GRCh38 chr8: 6,871,746-7,106,683 , GRCh37.p13 chr8: 6,729,268-6,964,205 DEFA3, DEFT1P2, 15 more genes
    nsv5478494copy number variation1nstd206human GRCh38 chr8: 6,225,437-7,016,330 , GRCh37.p13 chr8: 6,082,958-6,873,852 MCPH1-AS1, DEFB1, 23 more genes
    nsv5312107copy number variation1nstd204human GRCh38.p13 chr8: 6,711,695-7,028,836 , GRCh37.p13 chr8: 6,569,216-6,886,358 XKR5, DEFA1B, 18 more genes
    nsv5302903copy number variation1nstd204human GRCh38.p13 chr8: 6,544,839-6,937,873 , GRCh37.p13 chr8: 6,402,360-6,795,395 LOC100422495, MCPH1, 13 more genes
    nsv5249404copy number variation1nstd204human GRCh38.p13 chr8: 6,730,601-6,938,000 , GRCh37.p13 chr8: 6,588,122-6,795,522 XKR5, DEFA6, 8 more genes
    nsv5242218copy number variation1nstd204human GRCh38.p13 chr8: 6,711,701-6,991,300 , GRCh37.p13 chr8: 6,569,222-6,848,822 DEFA8P, DEFA6, 14 more genes
    nsv5240835copy number variation1nstd204human GRCh38.p13 chr8: 6,901,628-6,938,760 , GRCh37.p13 chr8: 6,759,150-6,796,282 DEFA4, DEFA6
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5182677mobile element insertion1nstd203human GRCh38 chr8: 6,924,586-6,924,601 , GRCh37.p13 chr8: 6,782,108-6,782,123 DEFA6
    nsv4969020copy number variation1nstd200human GRCh38 chr8: 6,544,849-6,937,869 , GRCh37.p13 chr8: 6,402,370-6,795,391 DEFA6, ANGPT2, 13 more genes
    nsv4958859copy number variation1nstd200human GRCh38 chr8: 6,919,370-6,923,981 , GRCh37.p13 chr8: 6,776,892-6,781,503 DEFA6
    nsv4825594copy number variation1nstd200human GRCh37 chr8: 6,569,224-6,886,349 , GRCh38.p12 chr8|NW_018654717.1: 106,973-423,951 , GRCh38.p12 chr8: 6,711,703-7,028,827 MIR4659A, DEFT1P2, 18 more genes
    nsv4825593copy number variation1nstd200human GRCh37 chr8: 6,402,370-6,795,391 , GRCh38.p12 chr8|NW_018654717.1: 1-332,992 , GRCh38.p12 chr8: 6,544,849-6,937,869 ANGPT2, XKR5, 13 more genes
    nsv4729120copy number variation1nstd102humanPathogenic GRCh37 chr8: 411,691-6,999,114 , GRCh38.p12 chr8: 461,691-7,141,592 LOC105377795, AGPAT5, 81 more genes
    nsv4685988copy number variation1nstd102humanPathogenic GRCh37 chr8: 161,516-11,516,619 , GRCh38.p12 chr8: 211,516-11,659,110 ZNF705B, RNU6-682P, 232 more genes
    nsv4680899copy number variation1nstd189human GRCh37.p13 chr8: 6,632,596-7,268,497 , GRCh38.p12 chr8: 6,775,075-7,410,975 DEFA1, DEFA3, 40 more genes
    nsv4679803copy number variation1nstd189human GRCh37.p13 chr8: 6,656,515-6,921,686 , GRCh38.p12 chr8: 6,798,994-7,064,164 , GRCh38.p12 chr8|NW_018654717.1: 194,263-459,291 DEFA1, DEFA3, 16 more genes
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