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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5673568copy number variation1nstd102humanPathogenic GRCh37 chr4: 151,336,570-151,520,303 , GRCh38.p12 chr4: 150,415,418-150,599,151 LOC100419161, LRBA, 2 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5465484copy number variation1nstd206human GRCh38 chr4: 150,558,924-150,577,720 , GRCh37.p13 chr4: 151,480,076-151,498,872 LOC729558, LRBA
    nsv5381428copy number variation1nstd102humanUncertain significance GRCh37 chr4: 151,336,570-151,604,889 , GRCh38.p12 chr4: 150,415,418-150,683,737 MAB21L2, LOC100419161, 2 more genes
    nsv5235385copy number variation1nstd204human GRCh38.p13 chr4: 150,574,401-150,577,700 , GRCh37.p13 chr4: 151,495,553-151,498,852 LRBA, LOC729558
    nsv4929628copy number variation1nstd200human GRCh38 chr4: 150,535,840-150,609,700 , GRCh37.p13 chr4: 151,456,992-151,530,852 LRBA, LOC729558, 1 more genes
    nsv4801130copy number variation1nstd200human GRCh37 chr4: 151,456,992-151,530,852 , GRCh38.p12 chr4: 150,535,840-150,609,700 MAB21L2, LOC729558, 1 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
    nsv4685732copy number variation1nstd102humanPathogenic GRCh37 chr4: 151,441,408-151,719,830 , GRCh38.p12 chr4: 150,520,256-150,798,678 MAB21L2, LOC729558, 2 more genes
    nsv4683860copy number variation1nstd102humanPathogenic GRCh37 chr4: 151,336,570-151,738,429 , GRCh38.p12 chr4: 150,415,418-150,817,277 MAB21L2, LOC729558, 3 more genes
    nsv4457244copy number variation1nstd102humanPathogenic GRCh37 chr4: 151,174,061-190,957,473 , GRCh38.p12 chr4: 150,252,909-190,036,318 LOC105377509, MIR3140, 487 more genes
    nsv4457046copy number variation1nstd102humanUncertain significance GRCh37 chr4: 151,276,833-151,511,404 , GRCh38.p12 chr4: 150,355,681-150,590,252 LRBA, LOC100419161, 2 more genes
    nsv4455420copy number variation1nstd102humanUncertain significance GRCh37 chr4: 151,428,984-151,807,861 , GRCh38.p12 chr4: 150,507,832-150,886,709 MAB21L2, ZBTB8OSP1, 2 more genes
    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
    nsv4372349copy number variation1nstd173human GRCh37 chr4: 151,135,128-153,328,827 , GRCh38.p12 chr4: 150,213,976-152,407,675 LOC105377489, FHIP1A-DT, 30 more genes
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