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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5874111copy number variation1nstd209human GRCh38 chr2: 95,406,564-95,406,672 , GRCh37.p13 chr2: 96,072,312-96,072,420 FAHD2A
    nsv5621812insertion1nstd207human GRCh38 chr2: 95,413,342-95,413,342 , GRCh37.p13 chr2: 96,079,090-96,079,090 FAHD2A
    nsv5575770copy number variation1nstd207human GRCh38 chr2: 95,414,296-95,414,452 , GRCh37.p13 chr2: 96,080,044-96,080,200 FAHD2A
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5212755copy number variation1nstd204human GRCh38.p13 chr2: 95,407,601-95,424,581 , GRCh37.p13 chr2: 96,073,349-96,090,329 FAHD2A
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4908124copy number variation1nstd200human GRCh38 chr2: 95,385,262-95,505,431 , GRCh37.p13 chr2: 96,051,010-96,171,179 KCNIP3, FAHD2A, 4 more genes
    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
    nsv4586779copy number variation1nstd183human GRCh37 chr2: 96,081,973-96,259,212 , GRCh38.p12 chr2: 95,416,225-95,593,464 , LOC100421287, 10 more genes
    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
    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
    nsv4067560copy number variation1nstd166human GRCh37.p13 chr2: 95,800,000-96,096,000 , GRCh38.p12 chr2: 95,134,255-95,430,252 ZNF2, KCNIP3, 7 more genes
    nsv4062982copy number variation1nstd166human GRCh37.p13 chr2: 96,074,303-96,074,607 , GRCh38.p12 chr2: 95,408,555-95,408,859 FAHD2A
    nsv4061432copy number variation1nstd166human GRCh37.p13 chr2: 96,073,000-96,080,800 , GRCh38.p12 chr2: 95,407,252-95,415,052 FAHD2A
    nsv4057213copy number variation1nstd166human GRCh37.p13 chr2: 96,066,000-96,071,000 , GRCh38.p12 chr2: 95,400,252-95,405,252 FAHD2A
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