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Items: 1 to 20 of 213

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148186copy number variation1nstd102humanUncertain significance GRCh37 chr20: 52,773,668-62,965,020 , GRCh38.p12 chr20: 54,157,129-64,333,667 LOC105372717, CTCFL, 245 more genes
    nsv7096265copy number variation1nstd102humanUncertain significance GRCh37 chr20: 60,854,193-60,886,170 , GRCh38.p12 chr20: 62,279,137-62,311,114 LAMA5, OSBPL2, 1 more genes
    nsv7096264copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,680,869 , GRCh38.p12 chr20: 62,256,185-64,049,516 RPS21, MIR1-1HG, 102 more genes
    nsv7095800copy number variation1nstd102humanUncertain significance GRCh37 chr20: 60,861,619-60,890,283 , GRCh38.p12 chr20: 62,286,563-62,315,227 ADRM1, OSBPL2, 1 more genes
    nsv7037078copy number variation1nstd229human GRCh38 chr20: 54,988,450-63,850,628 , GRCh37.p13 chr20: 53,604,989-62,481,981 , RPL39P, 209 more genes
    nsv7033732copy number variation1nstd229human GRCh38 chr20: 62,292,913-62,386,907 , GRCh37.p13 chr20: 60,867,969-60,961,963 ADRM1, LOC105372708, 6 more genes
    nsv7028397copy number variation1nstd229human GRCh38 chr20: 62,288,582-62,337,866 , GRCh37.p13 chr20: 60,863,638-60,912,922 MIR4758, LAMA5, 2 more genes
    nsv6637836copy number variation1nstd102humanUncertain significance GRCh37 chr20: 60,621,074-62,915,555 , GRCh38.p12 chr20: 62,046,018-64,284,202 SLC17A9, MIR3195, 120 more genes
    nsv6626604copy number variation1nstd224human GRCh37 chr20: 60,872,280-60,926,821 , GRCh38.p12 chr20: 62,297,224-62,351,765 MIR4758, LAMA5, 2 more genes
    nsv6546982copy number variation1nstd223human GRCh38 chr20: 62,292,913-62,386,907 , GRCh37.p13 chr20: 60,867,969-60,961,963 RPS21, ADRM1, 6 more genes
    nsv6315308copy number variation1nstd102humanUncertain significance GRCh38 chr20: 61,800,345-63,644,611 , GRCh37.p13 chr20: 60,375,401-62,275,964 STMN3, RPS21, 86 more genes
    nsv6314208copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,835,739-62,915,555 , GRCh38.p12 chr20: 58,260,683-64,284,202 LOC105372698, LOC105372695, 176 more genes
    nsv6283433copy number variation1nstd214human GRCh38 chr20: 62,304,017-62,304,087 , GRCh37.p13 chr20: 60,879,073-60,879,143 , ADRM1
    nsv6134311copy number variation1nstd213human GRCh37 chr20: 59,780,000-61,210,001 , GRCh38.p12 chr20: 61,204,944-62,612,794 LAMA5, PSMA7, 34 more genes
    nsv6134308copy number variation1nstd213human GRCh37 chr20: 55,660,000-60,880,001 , GRCh38.p12 chr20: 57,084,944-62,304,945 TAF4, OSBPL2, 97 more genes
    nsv6134085copy number variation1nstd213human GRCh37 chr20: 60,880,000-61,070,001 , GRCh38.p12 chr20: 62,304,944-62,494,945 LOC105372709, RBBP8NL, 10 more genes
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5514506copy number variation1nstd206human GRCh38 chr20: 62,307,924-62,308,630 , GRCh37.p13 chr20: 60,882,980-60,883,686 , LAMA5, 1 more genes
    nsv5381223copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,664,346 , GRCh38.p12 chr20: 62,256,185-64,032,993 KCNQ2-AS1, HAR1B, 100 more genes
    nsv5289201copy number variation1nstd204human GRCh38.p13 chr20: 62,058,601-62,909,300 , GRCh37.p13 chr20: 60,633,657-61,540,652 , LOC105372716, 47 more genes
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