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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053923inversion1nstd229human GRCh38 chr4: 143,521,980-150,843,613 , GRCh37.p13 chr4: 144,443,133-151,764,765 AKIRIN2P1, PRMT9, 87 more genes
    nsv7050914inversion1nstd229human GRCh38 chr4: 143,519,295-150,840,265 , GRCh37.p13 chr4: 144,440,448-151,761,417 MIR548G, LOC100420464, 87 more genes
    nsv6757117copy number variation1nstd229human GRCh38 chr4: 146,108,700-146,229,704 , GRCh37.p13 chr4: 147,029,852-147,150,856 REELD1, LINC01095, 2 more genes
    nsv6386890copy number variation1nstd223human GRCh38 chr4: 145,932,595-146,233,198 , GRCh37.p13 chr4: 146,853,747-147,154,350 REELD1, LOC105377469, 4 more genes
    nsv6311715copy number variation1nstd102humanPathogenic GRCh37 chr4: 146,560,292-149,358,012 , GRCh38.p12 chr4: 145,639,140-148,436,860 PRMT5P1, LOC105377472, 32 more genes
    nsv6134884copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,720,001 , GRCh38.p12 chr4: 108,308,844-160,798,849 , ANK2, 616 more genes
    nsv6134731copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,710,001 , GRCh38.p12 chr4: 108,308,844-160,788,849 , ANK2, 616 more genes
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv6060773insertion1nstd212human GRCh38 chr4: 146,104,185-146,104,185 , GRCh37.p13 chr4: 147,025,337-147,025,337 LOC105377469
    nsv5995255copy number variation1nstd212human GRCh38 chr4: 146,104,192-146,104,247 , GRCh37.p13 chr4: 147,025,344-147,025,399 LOC105377469
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv4948535copy number variation1nstd200human GRCh38 chr4: 145,932,520-146,233,308 , GRCh37.p13 chr4: 146,853,672-147,154,460 , LOC105377468, 5 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4733336copy number variation1nstd199human GRCh37 chr4: 147,025,323-147,025,388 , GRCh38.p12 chr4: 146,104,171-146,104,236 LOC105377469
    nsv4654172copy number variation1nstd186human GRCh37 chr4: 147,026,623-147,027,414 , GRCh38.p12 chr4: 146,105,471-146,106,262 LOC105377469
    nsv4455301copy number variation1nstd102humanPathogenic GRCh37 chr4: 124,873,497-185,278,662 , GRCh38.p12 chr4: 123,952,342-184,357,509 SMARCA5, SFRP2, 633 more genes
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