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Items: 1 to 20 of 429

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097596copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 88,258,289-88,279,328 , GRCh38.p12 chr6: 87,548,571-87,569,610 RARS2
    nsv7097595copy number variation1nstd102humanPathogenic GRCh37 chr6: 88,226,514-88,231,252 , GRCh38.p12 chr6: 87,516,796-87,521,534 RARS2
    nsv7097462copy number variation1nstd102humanUncertain significance GRCh37 chr6: 88,182,722-88,229,994 , GRCh38.p12 chr6: 87,473,004-87,520,276 SLC35A1, RNU6-444P, 1 more genes
    nsv7093441delins1nstd102humanPathogenic GRCh37 chr6: 88,228,358-88,228,358 , GRCh38 chr6: 87,518,640-87,518,640 RARS2
    nsv7039342inversion1nstd229human GRCh38 chr6: 86,041,090-92,871,248 , GRCh37.p13 chr6: 86,750,808-93,580,966 NDUFA5P9, AKIRIN2, 85 more genes
    nsv6814938copy number variation1nstd229human GRCh38 chr6: 87,580,758-87,584,931 , GRCh37.p13 chr6: 88,290,476-88,294,649 RARS2
    nsv6814550copy number variation1nstd229human GRCh38 chr6: 87,443,412-87,700,431 , GRCh37.p13 chr6: 88,153,130-88,410,149 RARS2, CFAP206, 5 more genes
    nsv6814405copy number variation1nstd229human GRCh38 chr6: 87,580,801-87,584,900 , GRCh37.p13 chr6: 88,290,519-88,294,618 RARS2
    nsv6813583copy number variation1nstd229human GRCh38 chr6: 87,566,485-87,570,501 , GRCh37.p13 chr6: 88,276,203-88,280,219 RARS2
    nsv6813419copy number variation1nstd229human GRCh38 chr6: 87,552,701-87,566,900 , GRCh37.p13 chr6: 88,262,419-88,276,618 RARS2
    nsv6813406copy number variation1nstd229human GRCh38 chr6: 87,507,114-87,624,272 , GRCh37.p13 chr6: 88,216,832-88,333,990 SLC35A1, ORC3, 1 more genes
    nsv6811298copy number variation1nstd229human GRCh38 chr6: 87,539,536-87,542,372 , GRCh37.p13 chr6: 88,249,254-88,252,090 RARS2
    nsv6809572copy number variation1nstd229human GRCh38 chr6: 87,541,368-87,544,134 , GRCh37.p13 chr6: 88,251,086-88,253,852 RARS2
    nsv6808968copy number variation1nstd229human GRCh38 chr6: 87,583,501-87,591,900 , GRCh37.p13 chr6: 88,293,219-88,301,618 RARS2, ORC3
    nsv6807349copy number variation1nstd229human GRCh38 chr6: 87,330,250-87,595,767 , GRCh37.p13 chr6: 88,039,968-88,305,485 RARS2, LOC100420741, 10 more genes
    nsv6805152copy number variation1nstd229human GRCh38 chr6: 87,567,201-87,606,400 , GRCh37.p13 chr6: 88,276,919-88,316,118 ORC3, RARS2
    nsv6805012copy number variation1nstd229human GRCh38 chr6: 87,543,365-87,543,432 , GRCh37.p13 chr6: 88,253,083-88,253,150 RARS2
    nsv6804933copy number variation1nstd229human GRCh38 chr6: 87,461,833-87,585,679 , GRCh37.p13 chr6: 88,171,551-88,295,397 SLC35A1, RNU6-444P, 2 more genes
    nsv6801357copy number variation1nstd229human GRCh38 chr6: 87,577,101-87,581,800 , GRCh37.p13 chr6: 88,286,819-88,291,518 RARS2
    nsv6800565copy number variation1nstd229human GRCh38 chr6: 87,576,087-87,576,564 , GRCh37.p13 chr6: 88,285,805-88,286,282 RARS2
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