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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5877871copy number variation1nstd209human GRCh38 chr2: 95,270,633-95,272,569 , GRCh37.p13 chr2: 95,936,381-95,938,317 PROM2
    nsv5834135copy number variation1nstd209human GRCh38 chr2: 95,270,588-95,272,587 , GRCh37.p13 chr2: 95,936,336-95,938,335 PROM2
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5290565copy number variation1nstd204human GRCh38.p13 chr2: 95,270,613-95,272,590 , GRCh37.p13 chr2: 95,936,361-95,938,338 PROM2
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4908121copy number variation1nstd200human GRCh38 chr2: 95,270,635-95,272,570 , GRCh37.p13 chr2: 95,936,383-95,938,318 PROM2
    nsv4777062copy number variation1nstd200human GRCh37 chr2: 95,936,383-95,938,318 , GRCh38.p12 chr2: 95,270,635-95,272,570 PROM2
    nsv4766632inversion1nstd199human GRCh37 chr2: 87,997,505-112,010,501 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,697,986-111,252,924 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 706 more genes
    nsv4752571inversion1nstd199human GRCh37 chr2: 87,550,795-112,295,517 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,323,672-111,537,940 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 723 more genes
    nsv4743379copy number variation1nstd199human GRCh37 chr2: 88,481,090-124,440,189 , GRCh38.p12 chr9: 40,649,751-63,450,622 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 88,181,571-123,682,613 , EIF2AK3, 861 more genes
    nsv4673887copy number variation2nstd102humanUncertain significance GRCh37 chr2: 95,930,035-96,755,045 , GRCh38.p12 chr2: 95,264,287-96,089,297 ANKRD33BP1, FABP7P2, 24 more genes
    nsv4664356copy number variation1nstd186human GRCh37 chr2: 95,952,650-95,952,694 , GRCh38.p12 chr2: 95,286,902-95,286,946 PROM2
    nsv4659269copy number variation1nstd186human GRCh37 chr2: 95,936,381-95,938,318 , GRCh38.p12 chr2: 95,270,633-95,272,570 PROM2
    nsv4586778copy number variation1nstd183human GRCh37 chr2: 95,936,381-95,938,318 , GRCh38.p12 chr2: 95,270,633-95,272,570 PROM2
    nsv4584729copy number variation2nstd183human GRCh37 chr2: 95,952,650-95,952,694 , GRCh38.p12 chr2: 95,286,902-95,286,946 PROM2
    nsv4453674copy number variation1nstd102humanUncertain significance GRCh37 chr2: 95,800,306-96,097,247 , GRCh38.p12 chr2: 95,134,561-95,431,499 ZNF2, FAHD2A, 7 more genes
    nsv4451325copy number variation1nstd102humanUncertain significance GRCh37 chr2: 95,476,818-96,193,825 , GRCh38.p12 chr2: 94,811,073-95,528,077 FAHD2A, LOC100287523, 25 more genes
    nsv4409239copy number variation1nstd174human GRCh37 chr2: 95,936,359-95,938,318 , GRCh38.p12 chr2: 95,270,611-95,272,570 PROM2
    nsv4405670copy number variation1nstd174human GRCh37 chr2: 95,913,278-96,400,008 , GRCh38.p12 chr2: 95,247,530-95,734,260 , PROM2, 18 more genes
    nsv4071678copy number variation1nstd166human GRCh37.p13 chr2: 95,921,000-96,144,000 , GRCh38.p12 chr2: 95,255,252-95,478,252 KCNIP3, FAHD2A, 5 more genes
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