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Items: 1 to 20 of 257

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963645insertion1nstd209human GRCh38 chr3: 170,525,629-170,525,629 , GRCh37.p13 chr3: 170,243,418-170,243,418 SLC7A14-AS1, SLC7A14
    nsv5905565copy number variation1nstd209human GRCh38 chr3: 170,532,166-170,532,301 , GRCh37.p13 chr3: 170,249,955-170,250,090 SLC7A14-AS1, SLC7A14
    nsv5901891copy number variation1nstd209human GRCh38 chr3: 170,460,656-170,461,032 , GRCh37.p13 chr3: 170,178,444-170,178,820 SLC7A14
    nsv5687815mobile element insertion2nstd211human GRCh38 chr3: 170,510,400-170,510,400 , GRCh37.p13 chr3: 170,228,189-170,228,189 SLC7A14, SLC7A14-AS1
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5450311copy number variation1nstd206human GRCh38 chr3: 170,472,022-170,472,093 , GRCh37.p13 chr3: 170,189,810-170,189,881 SLC7A14-AS1, SLC7A14
    nsv5449502copy number variation1nstd206human GRCh38 chr3: 170,534,326-170,534,651 , GRCh37.p13 chr3: 170,252,115-170,252,440 SLC7A14, SLC7A14-AS1
    nsv5440341copy number variation1nstd206human GRCh38 chr3: 170,532,169-170,532,302 , GRCh37.p13 chr3: 170,249,958-170,250,091 SLC7A14-AS1, SLC7A14
    nsv5313270copy number variation1nstd204human GRCh37.p13 chr3: 170,249,935-170,250,113 , GRCh38.p13 chr3: 170,532,146-170,532,324 SLC7A14-AS1, SLC7A14
    nsv5165828mobile element insertion1nstd203human GRCh38 chr3: 170,582,286-170,582,303 , GRCh37.p13 chr3: 170,300,075-170,300,092 SLC7A14-AS1, SLC7A14
    nsv5094234mobile element insertion1nstd203human GRCh38 chr3: 170,512,659-170,512,681 , GRCh37.p13 chr3: 170,230,448-170,230,470 SLC7A14-AS1, SLC7A14
    nsv5085532mobile element insertion1nstd203human GRCh38 chr3: 170,512,681-170,512,727 , GRCh37.p13 chr3: 170,230,470-170,230,516 SLC7A14-AS1, SLC7A14
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4920671copy number variation1nstd200human GRCh38 chr3: 170,462,508-170,462,658 , GRCh37.p13 chr3: 170,180,296-170,180,446 SLC7A14
    nsv4798538copy number variation1nstd200human GRCh37 chr3: 170,186,370-170,186,672 , GRCh38.p12 chr3: 170,468,582-170,468,884 SLC7A14-AS1, SLC7A14
    nsv4798537copy number variation1nstd200human GRCh37 chr3: 170,178,446-170,178,821 , GRCh38.p12 chr3: 170,460,658-170,461,033 SLC7A14
    nsv4674680copy number variation1nstd102humanPathogenic GRCh37 chr3: 169,617,690-190,593,854 , GRCh38.p12 chr3: 169,899,902-190,876,065 RNU6-1120P, LOC105374262, 323 more genes
    nsv4556229insertion1nstd166human GRCh37.p13 chr3: 170,243,417-170,243,417 , GRCh38.p12 chr3: 170,525,628-170,525,628 SLC7A14, SLC7A14-AS1
    nsv4550461insertion1nstd166human GRCh37.p13 chr3: 170,199,856-170,199,856 , GRCh38.p12 chr3: 170,482,067-170,482,067 SLC7A14-AS1, SLC7A14
    nsv4470250mobile element insertion1nstd166human GRCh37.p13 chr3: 170,274,008-170,274,008 , GRCh38.p12 chr3: 170,556,219-170,556,219 SLC7A14-AS1, SLC7A14
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