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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112750copy number variation1nstd102humanPathogenic GRCh37 chr2: 81,209,244-86,688,030 , GRCh38.p12 chr2: 80,982,120-86,460,907 VAMP8, TMSB10, 86 more genes
    nsv5974407inversion1nstd209human GRCh38 chr2: 81,628,747-84,582,693 , GRCh37.p13 chr2: 81,855,871-84,809,817 DHFRP3, DNAH6, 24 more genes
    nsv5875045copy number variation1nstd209human GRCh38 chr2: 83,501,327-83,522,717 , GRCh37.p13 chr2: 83,728,451-83,749,841 LOC105374834, LINC01809
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5440815copy number variation1nstd206human GRCh38 chr2: 83,007,834-83,636,924 , GRCh37.p13 chr2: 83,234,958-83,864,048 LINC01809, LOC112268410, 3 more genes
    nsv5360863translocation1nstd200human GRCh38 chr2: 83,522,546-83,522,546 , GRCh38 chr2: 83,522,456-83,522,456 , GRCh37.p13 chr2: 83,749,670-83,749,670 , GRCh37.p13 chr2: 83,749,580-83,749,580 LINC01809, LOC105374834
    nsv5036683inversion1nstd200human GRCh38 chr2: 81,353,883-84,286,769 , GRCh37.p13 chr2: 81,581,007-84,513,893 CHMP4AP1, MTND6P7, 24 more genes
    nsv4902297copy number variation1nstd200human GRCh38 chr2: 83,518,658-83,522,738 , GRCh37.p13 chr2: 83,745,782-83,749,862 LINC01809, LOC105374834
    nsv4902288copy number variation1nstd200human GRCh38 chr2: 83,350,094-83,736,249 , GRCh37.p13 chr2: 83,577,218-83,963,373 RPL37P10, LOC105374834, 2 more genes
    nsv4776838copy number variation1nstd200human GRCh37 chr2: 83,235,313-83,864,062 , GRCh38.p12 chr2: 83,008,189-83,636,938 LOC105374834, LOC112268410, 3 more genes
    nsv4728322copy number variation1nstd102humanUncertain significance GRCh37 chr2: 83,598,955-84,683,243 , GRCh38.p12 chr2: 83,371,831-84,456,119 FUNDC2P2, RNU6-1312P, 7 more genes
    nsv4679703copy number variation1nstd189human GRCh37.p13 chr2: 83,714,204-84,140,457 , GRCh38.p12 chr2: 83,487,080-83,913,333 RPL37P10, LINC01809, 2 more genes
    nsv4584586copy number variation1nstd183human GRCh37 chr2: 83,235,809-83,864,013 , GRCh38.p12 chr2: 83,008,685-83,636,889 RPL37P10, LINC01809, 3 more genes
    nsv4518871copy number variation1nstd166human GRCh37.p13 chr2: 83,715,888-84,208,167 , GRCh38.p12 chr2: 83,488,764-83,981,043 LINC01809, RNU6-1312P, 2 more genes
    nsv4451607copy number variation1nstd102humanPathogenic GRCh37 chr2: 77,907,114-87,330,965 , GRCh38.p12 chr2: 77,679,988-87,103,842 REEP1, RBX1P1, 134 more genes
    nsv4408805copy number variation1nstd174human GRCh37 chr2: 83,235,809-83,916,472 , GRCh38.p12 chr2: 83,008,685-83,689,348 RPL37P10, LINC01809, 4 more genes
    nsv4070258copy number variation1nstd166human GRCh37.p13 chr2: 83,452,274-83,770,593 , GRCh38.p12 chr2: 83,225,150-83,543,469 LINC01809, LOC105374834, 1 more genes
    nsv3916821copy number variation1nstd102humanPathogenic NCBI36 chr2: 47,701,031-86,783,356 , GRCh37.p13 chr2: 47,847,527-86,929,845 , GRCh38.p12 chr2: 47,620,388-86,702,722 NAGK, NRXN1-DT, 595 more genes
    nsv3915812copy number variation1nstd102humanBenign NCBI36 chr2: 83,117,096-83,658,069 , GRCh37.p13 chr2: 83,263,585-83,804,558 , GRCh38.p12 chr2: 83,036,461-83,577,434 LOC105374833, LINC01809, 2 more genes
    nsv3913121copy number variation1nstd102humanUncertain significance NCBI36 chr2: 83,588,915-83,963,589 , GRCh37.p13 chr2: 83,735,404-84,110,078 , GRCh38.p12 chr2: 83,508,280-83,882,954 RPL37P10, LINC01809, 2 more genes
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