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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5381149copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,333,802-51,195,728 , GRCh38.p12 chr22: 41,937,798-50,757,300 WBP2NL, RN7SKP80, 210 more genes
    nsv5035400copy number variation1nstd200human GRCh38 chr22: 44,436,410-45,546,334 , GRCh37.p13 chr22: 44,832,290-45,942,214 , RIBC2, 29 more genes
    nsv4729965copy number variation1nstd102humanUncertain significance GRCh37 chr22: 44,705,738-45,475,334 , GRCh38.p12 chr22: 44,309,858-45,079,453 LOC101927551, KRT18P23, 16 more genes
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4729920copy number variation1nstd102humanUncertain significance GRCh37 chr22: 44,795,975-45,297,787 , GRCh38.p12 chr22: 44,400,095-44,901,907 RTL6, LOC105373062, 13 more genes
    nsv4729777copy number variation1nstd102humanUncertain significance GRCh37 chr22: 44,649,786-45,866,882 , GRCh38.p12 chr22: 44,253,906-45,471,001 RIBC2, PHF21B, 27 more genes
    nsv4685945copy number variation1nstd102humanPathogenic GRCh38 chr22: 43,032,129-50,739,836 , GRCh37.p13 chr22: 43,428,135-51,178,264 LOC101927474, SHISAL1, 165 more genes
    nsv4685937copy number variation1nstd102humanPathogenic GRCh38 chr22: 43,802,117-50,806,121 , GRCh37.p13 chr22: 44,197,997-51,203,353 CIMAP1B, PNPLA3, 151 more genes
    nsv4685901copy number variation1nstd102humanPathogenic GRCh38 chr22: 44,245,760-50,806,121 , GRCh37.p13 chr22: 44,641,640-51,203,353 CHKB, TYMP, 141 more genes
    nsv4685771copy number variation1nstd102humanPathogenic GRCh37 chr22: 44,850,001-50,850,001 , GRCh38.p12 chr22: 44,454,121-50,411,572 LOC284933, EPIC1, 112 more genes
    nsv4676292copy number variation1nstd102humanPathogenic GRCh37 chr22: 30,654,764-51,197,838 , GRCh38.p12 chr22: 30,258,775-50,759,410 PDXP-DT, PDGFB, 550 more genes
    nsv4676232copy number variation1nstd102humanPathogenic GRCh37 chr22: 40,502,364-51,197,838 , GRCh38.p12 chr22: 40,106,360-50,759,410 MIR378I, SNORD13P1, 274 more genes
    nsv4676167copy number variation1nstd102humanUncertain significance GRCh37 chr22: 44,642,723-45,340,485 , GRCh38.p12 chr22: 44,246,843-44,944,605 LOC105373062, LINC00229, 15 more genes
    nsv4633801copy number variation1nstd183human GRCh37 chr22: 44,822,522-45,225,362 , GRCh38.p12 chr22: 44,426,642-44,829,482 LOC105373059, RTL6, 10 more genes
    nsv4457771copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410 IGLV3-27, XKR3, 1082 more genes
    nsv4351202copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,416,026-51,181,759 , GRCh38.p12 chr22: 42,020,022-50,743,331 PLXNB2, WBP2NL, 204 more genes
    nsv3924136copy number variation1nstd102humanPathogenic GRCh38 chr22: 40,202,014-50,735,806 , GRCh37 chr22: 40,598,018-51,174,234 , NCBI36 chr22: 38,927,964-49,521,100 CYP2D8P, TBC1D22A-AS1, 270 more genes
    nsv3923763copy number variation1nstd102humanPathogenic NCBI36 chr22: 42,534,579-49,525,130 , GRCh37 chr22: 44,203,246-51,178,264 , GRCh38 chr22: 43,807,366-50,739,836 EPIC1, PNPLA3, 147 more genes
    nsv3923135copy number variation1nstd102humanPathogenic GRCh38 chr22: 42,493,445-50,268,479 , GRCh37 chr22: 42,889,451-50,706,908 , NCBI36 chr22: 41,219,395-49,049,035 LINC01656, LOC107985537, 156 more genes
    nsv3920085copy number variation1nstd102humanBenign NCBI36 chr22: 42,720,092-49,468,408 , GRCh38 chr22: 43,992,879-50,683,114 , GRCh37 chr22: 44,388,759-51,121,542 MIR3667, CIMAP1B, 138 more genes
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