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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5880879copy number variation1nstd209human GRCh38 chr2: 98,469,455-98,469,758 , GRCh37.p13 chr2: 99,085,918-99,086,221 INPP4A
    nsv5880802copy number variation1nstd209human GRCh38 chr2: 98,593,253-98,593,308 , GRCh37.p13 chr2: 99,209,716-99,209,771 INPP4A
    nsv5871426copy number variation1nstd209human GRCh38 chr2: 98,593,884-98,593,935 , GRCh37.p13 chr2: 99,210,347-99,210,398 INPP4A
    nsv5870569copy number variation1nstd209human GRCh38 chr2: 98,583,770-98,583,820 , GRCh37.p13 chr2: 99,200,233-99,200,283 INPP4A
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5380548translocation1nstd200human GRCh38 chr2: 98,459,995-98,459,995 , GRCh38 chr2: 98,459,305-98,459,305 , GRCh37.p13 chr2: 99,075,768-99,075,768 , GRCh37.p13 chr2: 99,076,458-99,076,458 INPP4A
    nsv5063699mobile element insertion1nstd203human GRCh38 chr2: 98,453,372-98,453,386 , GRCh37.p13 chr2: 99,069,835-99,069,849 INPP4A
    nsv5061396mobile element insertion1nstd203human GRCh38 chr2: 98,515,499-98,515,513 , GRCh37.p13 chr2: 99,131,962-99,131,976 INPP4A
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4908237copy number variation1nstd200human GRCh38 chr2: 98,526,071-98,530,067 , GRCh37.p13 chr2: 99,142,534-99,146,530 INPP4A
    nsv4908236copy number variation1nstd200human GRCh38 chr2: 98,524,516-98,525,877 , GRCh37.p13 chr2: 99,140,979-99,142,340 INPP4A
    nsv4908235copy number variation1nstd200human GRCh38 chr2: 98,463,150-98,468,454 , GRCh37.p13 chr2: 99,079,613-99,084,917 INPP4A
    nsv4894838copy number variation1nstd200human GRCh38 chr2: 98,503,031-98,515,752 , GRCh37.p13 chr2: 99,119,494-99,132,215 INPP4A
    nsv4777149copy number variation1nstd200human GRCh37 chr2: 99,198,991-99,199,459 , GRCh38.p12 chr2: 98,582,528-98,582,996 INPP4A
    nsv4777148copy number variation1nstd200human GRCh37 chr2: 99,142,534-99,146,530 , GRCh38.p12 chr2: 98,526,071-98,530,067 INPP4A
    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
    nsv4737649copy number variation1nstd199human GRCh37 chr2: 99,121,361-99,127,790 , GRCh38.p12 chr2: 98,504,898-98,511,327 INPP4A
    nsv4518566copy number variation1nstd166human GRCh37.p13 chr2: 99,210,347-99,210,415 , GRCh38.p12 chr2: 98,593,884-98,593,952 INPP4A
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