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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5898771copy number variation1nstd209human GRCh38 chr3: 193,244,170-193,244,260 , GRCh37.p13 chr3: 192,961,959-192,962,049 PLAAT1, MGC2889
    nsv5681090mobile element insertion1nstd211human GRCh38 chr3: 193,240,930-193,240,930 , GRCh37.p13 chr3: 192,958,719-192,958,719 PLAAT1, MGC2889, 1 more genes
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5446769copy number variation1nstd206human GRCh38 chr3: 193,244,170-193,244,263 , GRCh37.p13 chr3: 192,961,959-192,962,052 PLAAT1, MGC2889
    nsv5399440mobile element insertion1nstd206human GRCh38 chr3: 193,240,930-193,240,981 , GRCh37.p13 chr3: 192,958,719-192,958,770 PLAAT1, MGC2889, 1 more genes
    nsv5352367translocation1nstd200human GRCh38 chr3: 193,244,170-193,244,170 , GRCh38 chr3: 193,244,263-193,244,263 , GRCh37.p13 chr3: 192,961,959-192,961,959 , GRCh37.p13 chr3: 192,962,052-192,962,052 PLAAT1, MGC2889
    nsv5087390mobile element insertion1nstd203human GRCh38 chr3: 193,240,915-193,240,930 , GRCh37.p13 chr3: 192,958,704-192,958,719 PLAAT1, MGC2889, 1 more genes
    nsv4925009copy number variation1nstd200human GRCh38 chr3: 193,087,867-193,424,977 , GRCh37.p13 chr3: 192,805,656-193,142,766 PLAAT1, ATP13A5-AS1, 5 more genes
    nsv4807188copy number variation1nstd200human GRCh37 chr3: 192,961,959-192,962,052 , GRCh38.p12 chr3: 193,244,170-193,244,263 MGC2889, PLAAT1
    nsv4585815copy number variation1nstd183human GRCh37 chr3: 192,886,435-193,292,130 , GRCh38.p12 chr3: 193,168,646-193,574,341 PLAAT1, ATP13A4, 5 more genes
    nsv4470824mobile element insertion1nstd166human GRCh37.p13 chr3: 192,958,704-192,958,704 , GRCh38.p12 chr3: 193,240,915-193,240,915 PLAAT1, MGC2889, 1 more genes
    nsv4469769mobile element insertion1nstd166human GRCh37.p13 chr3: 192,961,611-192,961,611 , GRCh38.p12 chr3: 193,243,822-193,243,822 PLAAT1, MGC2889
    nsv4436392copy number variation1nstd102humanPathogenic GRCh37 chr3: 188,386,566-197,838,262 , GRCh38.p12 chr3: 188,668,778-198,111,391 PPP1R2, GCNT1P3, 194 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4101105copy number variation1nstd166human GRCh37.p13 chr3: 192,961,959-192,962,052 , GRCh38.p12 chr3: 193,244,170-193,244,263 PLAAT1, MGC2889
    nsv3922385copy number variation1nstd102humanPathogenic NCBI36 chr3: 177,369,007-199,329,651 , GRCh37 chr3: 175,886,313-197,845,254 , GRCh38 chr3: 176,168,525-198,118,383 LINC02053, RTP4, 414 more genes
    nsv3921532copy number variation1nstd102humanPathogenic GRCh38 chr3: 190,667,663-198,110,178 , NCBI36 chr3: 191,868,146-199,321,446 , GRCh37 chr3: 190,385,452-197,837,049 LOC105374282, PIGX, 173 more genes
    nsv3920718copy number variation1nstd102humanPathogenic NCBI36 chr3: 188,646,713-196,231,151 , GRCh37 chr3: 187,164,019-194,749,862 , GRCh38 chr3: 187,446,231-195,029,133 LOC105374283, MIR944, 105 more genes
    nsv3920662copy number variation1nstd102humanPathogenic NCBI36 chr3: 178,729,187-199,321,446 , GRCh37.p13 chr3: 177,246,493-197,837,049 , GRCh38.p12 chr3: 177,528,705-198,110,178 RN7SKP265, RPL24P6, 401 more genes
    nsv3920607copy number variation1nstd102humanPathogenic NCBI36 chr3: 187,082,628-197,946,692 , GRCh37.p13 chr3: 185,599,934-196,462,295 , GRCh38.p12 chr3: 185,882,146-196,735,424 FGF12, RFC4, 212 more genes
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