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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148265copy number variation1nstd102humanPathogenic GRCh38 chr5: 176,447,531-177,312,407 , GRCh37.p13 chr5: 175,874,532-176,739,408 MXD3, FAF2, 19 more genes
    nsv7097523copy number variation2nstd102humanPathogenic GRCh37 chr5: 176,289,625-177,151,363 , GRCh38.p12 chr5: 176,862,624-177,724,362 PFN3, DBN1, 29 more genes
    nsv7097267copy number variation3nstd102humanUncertain significance GRCh37 chr5: 175,158,654-179,263,593 , GRCh38.p12 chr5: 175,731,651-179,836,593 LOC112267937, LMAN2, 122 more genes
    nsv7050002inversion1nstd229human GRCh38 chr5: 175,906,338-177,936,522 , GRCh37.p13 chr5: 175,333,341-177,363,523 PRR7, OR1X5P, 60 more genes
    nsv7041901inversion1nstd229human GRCh38 chr5: 175,920,087-179,128,938 , GRCh37.p13 chr5: 175,347,090-178,555,939 LOC100288803, NHP2, 98 more genes
    nsv7040659inversion1nstd229human GRCh38 chr5: 174,927,732-178,443,561 , GRCh37.p13 chr5: 174,354,735-177,870,562 RN7SKP148, FAM193B-DT, 90 more genes
    nsv7040549inversion1nstd229human GRCh38 chr5: 176,829,915-176,830,439 , GRCh37.p13 chr5: 176,256,916-176,257,440 UNC5A
    nsv7038290inversion1nstd229human GRCh38 chr5: 172,489,078-179,485,008 , GRCh37.p13 chr5: 171,916,082-178,912,009 ZFP2, NHP2, 168 more genes
    nsv6797888copy number variation1nstd229human GRCh38 chr5: 176,827,732-176,832,461 , GRCh37.p13 chr5: 176,254,733-176,259,462 UNC5A
    nsv6797467copy number variation1nstd229human GRCh38 chr5: 176,820,001-176,838,200 , GRCh37.p13 chr5: 176,247,002-176,265,201 UNC5A
    nsv6797040copy number variation1nstd229human GRCh38 chr5: 176,859,801-176,862,300 , GRCh37.p13 chr5: 176,286,802-176,289,301 UNC5A
    nsv6796734copy number variation1nstd229human GRCh38 chr5: 176,843,282-176,846,134 , GRCh37.p13 chr5: 176,270,283-176,273,135 UNC5A
    nsv6794840copy number variation1nstd229human GRCh38 chr5: 176,865,701-176,925,200 , GRCh37.p13 chr5: 176,292,702-176,352,201 UIMC1, HK3, 1 more genes
    nsv6793057copy number variation1nstd229human GRCh38 chr5: 176,624,975-176,860,934 , GRCh37.p13 chr5: 176,051,976-176,287,935 MIR4281, EIF4E1B, 4 more genes
    nsv6790004copy number variation1nstd229human GRCh38 chr5: 176,848,289-176,854,045 , GRCh37.p13 chr5: 176,275,290-176,281,046 UNC5A
    nsv6788395copy number variation1nstd229human GRCh38 chr5: 176,766,621-176,812,987 , GRCh37.p13 chr5: 176,193,622-176,239,988 UNC5A
    nsv6787140copy number variation1nstd229human GRCh38 chr5: 176,835,288-176,838,193 , GRCh37.p13 chr5: 176,262,289-176,265,194 UNC5A
    nsv6782160copy number variation1nstd229human GRCh38 chr5: 176,616,290-176,856,593 , GRCh37.p13 chr5: 176,043,291-176,283,594 MIR4281, LINC01574, 4 more genes
    nsv6781109copy number variation1nstd229human GRCh38 chr5: 176,813,831-176,967,313 , GRCh37.p13 chr5: 176,240,832-176,394,314 HK3, UNC5A, 1 more genes
    nsv6779969copy number variation1nstd229human GRCh38 chr5: 176,850,915-176,850,972 , GRCh37.p13 chr5: 176,277,916-176,277,973 UNC5A
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