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Items: 1 to 20 of 272

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5952070insertion1nstd209human GRCh38 chr1: 244,444,514-244,444,514 , GRCh37.p13 chr1: 244,607,816-244,607,816 ADSS2
    nsv5872649copy number variation1nstd209human GRCh38 chr1: 244,428,584-244,428,663 , GRCh37.p13 chr1: 244,591,886-244,591,965 ADSS2
    nsv5688918mobile element insertion2nstd211human GRCh38 chr1: 244,409,858-244,409,858 , GRCh37.p13 chr1: 244,573,160-244,573,160 ADSS2
    nsv5688392mobile element insertion1nstd211human GRCh38 chr1: 244,408,349-244,408,349 , GRCh37.p13 chr1: 244,571,651-244,571,651 ADSS2
    nsv5451403copy number variation1nstd206human GRCh38 chr1: 244,438,202-244,442,053 , GRCh37.p13 chr1: 244,601,504-244,605,355 ADSS2
    nsv5442435copy number variation1nstd206human GRCh38 chr1: 244,441,706-244,444,242 , GRCh37.p13 chr1: 244,605,008-244,607,544 ADSS2
    nsv5442202copy number variation1nstd206human GRCh38 chr1: 244,428,587-244,428,664 , GRCh37.p13 chr1: 244,591,889-244,591,966 ADSS2
    nsv5409671mobile element insertion1nstd206human GRCh38 chr1: 244,409,858-244,409,909 , GRCh37.p13 chr1: 244,573,160-244,573,211 ADSS2
    nsv5401791mobile element insertion1nstd206human GRCh38 chr1: 244,408,349-244,408,400 , GRCh37.p13 chr1: 244,571,651-244,571,702 ADSS2
    nsv5381296copy number variation1nstd102humanPathogenic GRCh37 chr1: 240,554,955-247,342,593 , GRCh38.p12 chr1: 240,391,655-247,179,291 RPL6P3, RN7SKP12, 108 more genes
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5076993mobile element insertion1nstd203human GRCh38 chr1: 244,444,465-244,444,514 , GRCh37.p13 chr1: 244,607,767-244,607,816 ADSS2
    nsv5073176mobile element insertion1nstd203human GRCh38 chr1: 244,409,850-244,409,858 , GRCh37.p13 chr1: 244,573,152-244,573,160 ADSS2
    nsv5067799mobile element insertion1nstd203human GRCh38 chr1: 244,409,843-244,409,858 , GRCh37.p13 chr1: 244,573,145-244,573,160 ADSS2
    nsv5066982mobile element insertion1nstd203human GRCh38 chr1: 244,444,504-244,444,514 , GRCh37.p13 chr1: 244,607,806-244,607,816 ADSS2
    nsv5064458mobile element insertion1nstd203human GRCh38 chr1: 244,422,392-244,422,406 , GRCh37.p13 chr1: 244,585,694-244,585,708 ADSS2
    nsv5062249mobile element insertion1nstd203human GRCh38 chr1: 244,444,514-244,444,536 , GRCh37.p13 chr1: 244,607,816-244,607,838 ADSS2
    nsv4785649copy number variation1nstd200human GRCh37 chr1: 244,604,664-244,607,867 , GRCh38.p12 chr1: 244,441,362-244,444,565 ADSS2
    nsv4684187copy number variation1nstd102humanPathogenic GRCh37 chr1: 210,152,794-249,218,992 , GRCh38.p12 chr1: 209,979,449-248,924,793 HLX-AS1, OPN3, 740 more genes
    nsv4674467copy number variation1nstd102humanUncertain significance GRCh37 chr1: 243,863,432-244,634,537 , GRCh38.p12 chr1: 243,700,130-244,471,235 LOC105373260, LOC105373258, 11 more genes
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