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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964392insertion1nstd209human GRCh38 chr2: 197,547,091-197,547,091 , GRCh37.p13 chr2: 198,411,815-198,411,815 MOB4, HSPE1-MOB4
    nsv5688633mobile element insertion2nstd211human GRCh38 chr2: 197,547,104-197,547,104 , GRCh37.p13 chr2: 198,411,828-198,411,828 MOB4, HSPE1-MOB4
    nsv5621300insertion1nstd207human GRCh38 chr2: 197,547,091-197,547,091 , GRCh37.p13 chr2: 198,411,815-198,411,815 HSPE1-MOB4, MOB4
    nsv5610350insertion1nstd207human GRCh38 chr2: 197,506,438-197,506,438 , GRCh37.p13 chr2: 198,371,162-198,371,162 HSPE1-MOB4
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5450333copy number variation1nstd206human GRCh38 chr2: 197,518,401-197,518,542 , GRCh37.p13 chr2: 198,383,125-198,383,266 HSPE1-MOB4, MOB4
    nsv5405671mobile element insertion1nstd206human GRCh38 chr2: 197,547,104-197,547,149 , GRCh37.p13 chr2: 198,411,828-198,411,873 HSPE1-MOB4, MOB4
    nsv5381571copy number variation1nstd102humanUncertain significance GRCh37 chr2: 198,351,760-198,363,582 , GRCh38.p12 chr2: 197,487,036-197,498,858 HSPE1, SNORA105B, 2 more genes
    nsv5194605mobile element insertion1nstd203human GRCh38 chr2: 197,506,914-197,506,914 , GRCh37.p13 chr2: 198,371,638-198,371,638 HSPE1-MOB4
    nsv5076060mobile element insertion1nstd203human GRCh38 chr2: 197,506,438-197,506,452 , GRCh37.p13 chr2: 198,371,162-198,371,176 HSPE1-MOB4
    nsv5075778mobile element insertion1nstd203human GRCh38 chr2: 197,547,091-197,547,104 , GRCh37.p13 chr2: 198,411,815-198,411,828 HSPE1-MOB4, MOB4
    nsv5075455mobile element insertion1nstd203human GRCh38 chr2: 197,547,096-197,547,104 , GRCh37.p13 chr2: 198,411,820-198,411,828 HSPE1-MOB4, MOB4
    nsv5069998mobile element insertion1nstd203human GRCh38 chr2: 197,535,666-197,535,681 , GRCh37.p13 chr2: 198,400,390-198,400,405 HSPE1-MOB4, MOB4
    nsv5069399mobile element insertion1nstd203human GRCh38 chr2: 197,547,095-197,547,104 , GRCh37.p13 chr2: 198,411,819-198,411,828 HSPE1-MOB4, MOB4
    nsv4913799copy number variation1nstd200human GRCh38 chr2: 197,487,307-197,518,619 , GRCh37.p13 chr2: 198,352,031-198,383,343 HSPE1-MOB4, HSPD1, 3 more genes
    nsv4910205copy number variation1nstd200human GRCh38 chr2: 197,528,806-197,530,164 , GRCh37.p13 chr2: 198,393,530-198,394,888 HSPE1-MOB4, MOB4
    nsv4910204copy number variation1nstd200human GRCh38 chr2: 197,499,074-197,502,543 , GRCh37.p13 chr2: 198,363,798-198,367,267 HSPD1, HSPE1-MOB4, 1 more genes
    nsv4795449copy number variation1nstd200human GRCh37 chr2: 198,393,530-198,394,886 , GRCh38.p12 chr2: 197,528,806-197,530,162 HSPE1-MOB4, MOB4
    nsv4795448copy number variation1nstd200human GRCh37 chr2: 198,363,798-198,367,267 , GRCh38.p12 chr2: 197,499,074-197,502,543 HSPE1, HSPE1-MOB4, 1 more genes
    nsv4768322copy number variation1nstd102humanPathogenic GRCh37 chr2: 197,359,024-201,383,462 , GRCh38.p12 chr2: 196,494,300-200,518,739 ANKRD44-DT, ATP5MC2P3, 48 more genes
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