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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5493018copy number variation1nstd206human GRCh38 chr9: 94,315,552-94,338,776 , GRCh37.p13 chr9: 97,077,834-97,101,058 NUTM2F, LOC100132077, 2 more genes
    nsv5492240copy number variation1nstd206human GRCh38 chr9: 94,318,000-94,352,552 , GRCh37.p13 chr9: 97,080,282-97,114,834 PTMAP12, LOC105376154, 3 more genes
    nsv5473938copy number variation1nstd206human GRCh38 chr9: 94,280,000-94,576,600 , GRCh37.p13 chr9: 97,042,282-97,338,882 LOC107987023, PCAT7, 12 more genes
    nsv5259664copy number variation1nstd204human GRCh38.p13 chr9: 94,316,101-94,317,400 , GRCh37.p13 chr9: 97,078,383-97,079,682 LOC105376154, NUTM2F
    nsv5252536copy number variation1nstd204human GRCh38.p13 chr9: 94,326,001-94,334,600 , GRCh37.p13 chr9: 97,088,283-97,096,882 NUTM2F, LOC100132077
    nsv5243861copy number variation1nstd204human GRCh38.p13 chr9: 94,319,120-94,332,690 , GRCh37.p13 chr9: 97,081,402-97,094,972 LOC105376154, LOC100132077, 1 more genes
    nsv5242029copy number variation1nstd204human GRCh38.p13 chr9: 94,328,370-94,331,189 , GRCh37.p13 chr9: 97,090,652-97,093,471 LOC100132077, NUTM2F
    nsv4684256copy number variation1nstd102humanPathogenic GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991 RPS26P37, MIR27B, 238 more genes
    nsv4684026copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 96,160,235-97,428,496 , GRCh38.p12 chr9: 93,397,953-94,666,214 FBP1, PHF2, 30 more genes
    nsv4676103copy number variation1nstd102humanPathogenic NCBI36 chr9: 95,946,863-99,986,314 , GRCh37.p13 chr9: 96,907,042-100,946,493 , GRCh38.p12 chr9: 94,144,760-98,184,211 MIR3074, LOC112268039, 108 more genes
    nsv4607418copy number variation1nstd183human GRCh37 chr9: 96,999,239-97,239,821 , GRCh38.p12 chr9: 94,236,957-94,477,539 VDAC1P11, ZNF169, 8 more genes
    nsv4605679copy number variation1nstd183human GRCh37 chr9: 97,068,893-97,089,175 , GRCh38.p12 chr9: 94,306,611-94,326,893 NUTM2F, LOC105376154
    nsv4527020copy number variation1nstd166human GRCh37.p13 chr9: 97,088,000-97,141,000 , GRCh38.p12 chr9: 94,325,718-94,378,718 LOC107987023, MFSD14B, 3 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4418864copy number variation1nstd174human GRCh37 chr9: 97,068,893-97,099,816 , GRCh38.p12 chr9: 94,306,611-94,337,534 NUTM2F, LOC100132077, 2 more genes
    nsv4415153copy number variation1nstd174human GRCh37 chr9: 96,999,227-97,356,950 , GRCh38.p12 chr9: 94,236,945-94,594,668 FBP2, NUTM2F, 13 more genes
    nsv4349215copy number variation1nstd102humanPathogenic GRCh37 chr9: 79,520,825-97,201,274 , GRCh38.p12 chr9: 76,905,909-94,438,992 SPATA31C1, LINC02893, 280 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4183997copy number variation1nstd166human GRCh37.p13 chr9: 97,086,000-97,091,000 , GRCh38.p12 chr9: 94,323,718-94,328,718 NUTM2F, LOC105376154
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