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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5683777mobile element insertion1nstd211human GRCh38 chr3: 190,317,284-190,317,284 , GRCh37.p13 chr3: 190,035,073-190,035,073 CLDN1, CLDN16
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5396492mobile element insertion1nstd206human GRCh38 chr3: 190,317,284-190,317,335 , GRCh37.p13 chr3: 190,035,073-190,035,124 CLDN16, CLDN1
    nsv5041325inversion1nstd200human GRCh38 chr3: 190,101,121-190,805,722 , GRCh37.p13 chr3: 189,818,910-190,523,511 P3H2, RN7SKP296, 10 more genes
    nsv4924993copy number variation1nstd200human GRCh38 chr3: 190,311,265-190,312,950 , GRCh37.p13 chr3: 190,029,054-190,030,739 CLDN1, CLDN16
    nsv4924992copy number variation1nstd200human GRCh38 chr3: 190,262,317-190,583,119 , GRCh37.p13 chr3: 189,980,106-190,300,908 IL1RAP, CLDN16, 2 more genes
    nsv4921417copy number variation1nstd200human GRCh38 chr3: 190,316,928-190,319,004 , GRCh37.p13 chr3: 190,034,717-190,036,793 CLDN1, CLDN16
    nsv4684178copy number variation1nstd102humanUncertain significance GRCh37 chr3: 189,906,773-190,473,124 , GRCh38.p12 chr3: 190,188,984-190,755,335 LINC02013, CCT6P4, 6 more genes
    nsv4679536copy number variation1nstd189human GRCh37.p13 chr3: 189,748,702-190,592,486 , GRCh38.p12 chr3: 190,030,913-190,874,697 IL1RAP, CLDN1, 12 more genes
    nsv4674680copy number variation1nstd102humanPathogenic GRCh37 chr3: 169,617,690-190,593,854 , GRCh38.p12 chr3: 169,899,902-190,876,065 RNU6-1120P, LOC105374262, 323 more genes
    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
    nsv4347470copy number variation1nstd102humanPathogenic GRCh37 chr3: 190,039,387-190,040,504 , GRCh38.p12 chr3: 190,321,598-190,322,715 CLDN1, CLDN16
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4102304copy number variation1nstd166human GRCh37.p13 chr3: 189,416,756-190,222,423 , GRCh38.p12 chr3: 189,698,967-190,504,634 TMEM207, RNU6-1109P, 8 more genes
    nsv3923340copy number variation1nstd102humanPathogenic GRCh38 chr3: 187,446,231-190,839,052 , GRCh37 chr3: 187,164,019-190,556,841 , NCBI36 chr3: 188,646,713-192,039,535 ENOPH1P1, LINC01991, 36 more genes
    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
    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
    nsv3920067copy number variation1nstd102humanPathogenic GRCh38 chr3: 189,265,371-198,110,178 , NCBI36 chr3: 190,465,854-199,321,446 , GRCh37 chr3: 188,983,160-197,837,049 OSTN-AS1, ACAP2, 188 more genes
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