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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3883109copy number variation1nstd102humanBenign GRCh37 chr4: 125,361,767-125,652,879 , GRCh38.p12 chr4: 124,440,612-124,731,724 ANKRD50, TECRP2, 1 more genes
    nsv3917126copy number variation1nstd102humanPathogenic GRCh38 chr4: 116,630,862-145,429,900 , NCBI36 chr4: 117,771,466-146,570,502 , GRCh37 chr4: 117,552,018-146,351,052 ANKRD50, SETD7, 294 more genes
    nsv6290265copy number variation1nstd102humanPathogenic GRCh37 chr4: 114,872,547-138,005,267 , GRCh38.p12 chr4: 113,951,391-137,084,113 ANKRD50, LOC105379404, 218 more genes
    nsv3922957copy number variation1nstd102humanPathogenic GRCh37 chr4: 118,273,037-134,486,822 , GRCh38 chr4: 117,351,881-133,565,667 , NCBI36 chr4: 118,492,485-134,706,272 ANKRD50, LOC102724158, 168 more genes
    nsv5381774copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,833,638-130,232,122 , GRCh38.p12 chr4: 115,912,482-129,310,967 ANKRD50, LOC112268469, 159 more genes
    nsv3879381copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,307,857-129,302,960 , GRCh38.p12 chr4: 115,386,701-128,381,805 ANKRD50, SAR1AP3, 153 more genes
    nsv6313750copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,888,785-129,649,979 , GRCh38.p12 chr4: 115,967,629-128,728,824 ANKRD50, LOC105377395, 152 more genes
    nsv3886342copy number variation1nstd102humanPathogenic GRCh37 chr4: 124,282,603-134,014,299 , GRCh38.p12 chr4: 123,361,448-133,093,144 ANKRD50, LOC105377416, 72 more genes
    nsv3922404copy number variation1nstd102humanPathogenic GRCh38 chr4: 124,055,204-126,331,108 , GRCh37 chr4: 124,976,359-127,252,263 , NCBI36 chr4: 125,195,809-127,471,713 ANKRD50, LOC105377408, 14 more genes
    nsv3873978copy number variation1nstd102humanPathogenic GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724 ANKRD50, LOC100422029, 2358 more genes
    nsv3876533copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611 ANKRD50, LOC100420289, 2347 more genes
    nsv3884499copy number variation1nstd102humanPathogenic GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286 ANKRD50, MTND4LP29, 2341 more genes
    nsv3880085copy number variation2nstd102humanPathogenic GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318 ANKRD50, LOC112268460, 2345 more genes
    nsv3883791copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495 ANKRD50, LOC105377343, 2341 more genes
    nsv3875534copy number variation1nstd102humanPathogenic GRCh37 chr4: 93,071,152-190,957,473 , GRCh38.p12 chr4: 92,150,001-190,036,318 ANKRD50, KLKB1, 1118 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 ANKRD50, SNHG27, 1091 more genes
    nsv3874596copy number variation1nstd102humanPathogenic GRCh37 chr4: 109,199,664-189,752,726 , GRCh38.p12 chr4: 108,278,508-188,831,572 ANKRD50, RPL6P12, 938 more genes
    nsv3924008copy number variation1nstd102humanPathogenic GRCh38 chr4: 118,065,569-190,042,639 , GRCh37 chr4: 118,986,724-190,828,225 , NCBI36 chr4: 119,206,172-191,200,788 ANKRD50, PPID, 828 more genes
    nsv3874610copy number variation1nstd102humanPathogenic GRCh37 chr4: 119,437,495-190,904,301 , GRCh38.p12 chr4: 118,516,340-189,983,146 ANKRD50, OTUD4, 813 more genes
    nsv3918110copy number variation1nstd102humanPathogenic NCBI36 chr4: 122,658,828-191,220,419 , GRCh38 chr4: 121,518,223-190,062,270 , GRCh37 chr4: 122,439,378-190,828,225 ANKRD50, SCRG1, 770 more genes
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