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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5903839copy number variation1nstd209human GRCh38 chr5: 79,180,365-84,539,350 , GRCh37.p13 chr5: 78,476,188-83,835,168 , ANKRD34B, 84 more genes
    nsv5898803copy number variation1nstd209human GRCh38 chr5: 81,234,780-81,234,831 , GRCh37.p13 chr5: 80,530,599-80,530,650 CKMT2
    nsv5687372mobile element insertion1nstd211human GRCh38 chr5: 81,241,458-81,241,458 , GRCh37.p13 chr5: 80,537,277-80,537,277 CKMT2-AS1, CKMT2
    nsv5466067copy number variation1nstd206human GRCh38 chr5: 81,239,573-81,240,485 , GRCh37.p13 chr5: 80,535,392-80,536,304 CKMT2, CKMT2-AS1
    nsv5368593translocation1nstd200human GRCh38 chr5: 81,250,571-81,250,571 , GRCh38 chr5: 81,238,988-81,238,988 , GRCh37.p13 chr5: 80,546,390-80,546,390 , GRCh37.p13 chr5: 80,534,807-80,534,807 CKMT2, CKMT2-AS1
    nsv5033775inversion1nstd200human GRCh38 chr5: 76,373,686-102,541,075 , GRCh37.p13 chr5: 75,669,511-101,876,779 , F2RL1, 331 more genes
    nsv4808913copy number variation1nstd200human GRCh37 chr5: 80,534,807-80,546,390 , GRCh38.p12 chr5: 81,238,988-81,250,571 CKMT2, CKMT2-AS1
    nsv4704167copy number variation1nstd195human GRCh37 chr5: 80,353,001-80,573,351 , GRCh38.p12 chr5: 81,057,182-81,277,532 CKMT2, RASGRF2, 1 more genes
    nsv4675820copy number variation1nstd102humanUncertain significance GRCh37 chr5: 79,528,733-80,545,287 , GRCh38.p12 chr5: 80,232,914-81,249,468 LINC01337, SERINC5, 23 more genes
    nsv4675667copy number variation1nstd102humanPathogenic GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166 LOC101929380, LIX1-AS1, 318 more genes
    nsv4674872copy number variation1nstd102humanUncertain significance GRCh37 chr5: 80,323,403-80,577,511 , GRCh38.p12 chr5: 81,027,584-81,281,692 CKMT2, RASGRF2, 1 more genes
    nsv4598291copy number variation1nstd183human GRCh37 chr5: 80,535,750-80,545,341 , GRCh38.p12 chr5: 81,239,931-81,249,522 CKMT2, CKMT2-AS1
    nsv4591725copy number variation1nstd183human GRCh37 chr5: 80,534,944-80,542,836 , GRCh38.p12 chr5: 81,239,125-81,247,017 CKMT2-AS1, CKMT2
    nsv4522917copy number variation1nstd166human GRCh37.p13 chr5: 80,500,895-80,601,050 , GRCh38.p12 chr5: 81,205,076-81,305,231 ZCCHC9, CKMT2, 2 more genes
    nsv4456925copy number variation1nstd102humanUncertain significance GRCh37 chr5: 80,501,001-80,600,333 , GRCh38.p12 chr5: 81,205,182-81,304,514 CKMT2, ZCCHC9, 2 more genes
    nsv4456362copy number variation1nstd102humanUncertain significance GRCh37 chr5: 79,664,621-80,767,791 , GRCh38.p12 chr5: 80,368,802-81,471,972 CKMT2, ANKRD34B, 17 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4393584copy number variation1nstd174human GRCh37 chr5: 80,530,229-80,545,354 , GRCh38.p12 chr5: 81,234,410-81,249,535 CKMT2, CKMT2-AS1
    nsv4328126inversion1nstd166human GRCh37.p13 chr5: 75,669,511-101,876,780 , GRCh38.p12 chr5: 76,373,686-102,541,076 , BHMT, 331 more genes
    nsv4124045copy number variation1nstd166human GRCh37.p13 chr5: 80,552,690-80,552,742 , GRCh38.p12 chr5: 81,256,871-81,256,923 CKMT2, CKMT2-AS1
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