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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
    nsv5902244copy number variation1nstd209human GRCh38 chr4: 156,014,074-164,864,480 , GRCh37.p13 chr4: 156,935,226-165,785,632 , MIR3688-1, 67 more genes
    nsv5838665copy number variation1nstd209human GRCh38 chr4: 164,762,782-164,794,415 , GRCh37.p13 chr4: 165,683,934-165,715,567 SMIM31, RNU6-668P
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5381776copy number variation1nstd102humanPathogenic GRCh37 chr4: 157,771,352-172,496,278 , GRCh38.p12 chr4: 156,850,200-171,575,127 LOC107986326, LOC107986240, 144 more genes
    nsv5039478inversion1nstd200human GRCh38 chr4: 158,116,539-168,149,530 , GRCh37.p13 chr4: 159,037,691-169,070,681 MIR4454, LOC105377520, 93 more genes
    nsv4948672copy number variation1nstd200human GRCh38 chr4: 164,039,828-165,202,299 , GRCh37.p13 chr4: 164,960,980-166,123,451 MARCHF1, TRIM61, 21 more genes
    nsv4794651copy number variation1nstd200human GRCh37 chr4: 165,528,213-165,786,417 , GRCh38.p12 chr4: 164,607,061-164,865,265 RNU6-284P, CHORDC1P3, 2 more genes
    nsv4794650copy number variation1nstd200human GRCh37 chr4: 165,517,729-165,786,548 , GRCh38.p12 chr4: 164,596,577-164,865,396 CHORDC1P3, RNU6-668P, 2 more genes
    nsv4794645copy number variation1nstd200human GRCh37 chr4: 164,960,980-166,123,451 , GRCh38.p12 chr4: 164,039,828-165,202,299 SMIM31, MARCHF1, 21 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
    nsv4674043copy number variation1nstd102humanPathogenic GRCh37 chr4: 165,010,461-190,957,473 , GRCh38.p12 chr4: 164,089,309-190,036,318 CYP4V2, ZFP42, 319 more genes
    nsv4587925copy number variation1nstd183human GRCh37 chr4: 165,698,141-165,834,290 , GRCh38.p12 chr4: 164,776,989-164,913,138 SMIM31, RNU6-668P, 1 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
    nsv4457131copy number variation1nstd102humanPathogenic GRCh37 chr4: 165,069,355-177,189,728 , GRCh38.p12 chr4: 164,148,203-176,268,577 LINC02269, NOL8P1, 140 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
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