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Items: 1 to 20 of 84

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057899inversion1nstd229human GRCh38 chr3: 32,727,416-33,178,209 , GRCh37.p13 chr3: 32,768,908-33,219,701 TRIM71, TMPPE, 11 more genes
    nsv7046617inversion1nstd229human GRCh38 chr3: 32,574,554-33,118,910 , GRCh37.p13 chr3: 32,616,046-33,160,402 GLB1, LOC107986072, 12 more genes
    nsv7043797inversion1nstd229human GRCh38 chr3: 33,078,011-33,090,117 , GRCh37.p13 chr3: 33,119,503-33,131,609 GLB1, TMPPE, 1 more genes
    nsv7043212inversion1nstd229human GRCh38 chr3: 33,096,360-33,096,400 , GRCh37.p13 chr3: 33,137,852-33,137,892 TMPPE, GLB1
    nsv6705706copy number variation1nstd229human GRCh38 chr3: 33,087,489-33,112,622 , GRCh37.p13 chr3: 33,128,981-33,154,114 TMPPE, RN7SL296P, 2 more genes
    nsv6371270copy number variation1nstd223human GRCh38 chr3: 33,086,301-33,293,000 , GRCh37.p13 chr3: 33,127,793-33,334,492 RN7SL296P, GLB1, 4 more genes
    nsv6313757copy number variation1nstd102humanUncertain significance GRCh37 chr3: 32,699,328-35,286,114 , GRCh38.p12 chr3: 32,657,836-35,244,622 CRTAP, FECHP1, 26 more genes
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 LOC102724104, CRIP1P2, 291 more genes
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4793920copy number variation1nstd200human GRCh37 chr3: 32,391,980-33,567,070 , GRCh38.p12 chr3: 32,350,488-33,525,578 , RPL30P4, 25 more genes
    nsv4682517copy number variation1nstd102humanPathogenic GRCh37 chr3: 33,138,493-33,138,587 , GRCh38.p12 chr3: 33,097,001-33,097,095 GLB1, TMPPE
    nsv4588541copy number variation1nstd183human GRCh37 chr3: 33,138,251-33,138,658 , GRCh38.p12 chr3: 33,096,759-33,097,166 GLB1, TMPPE
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4452552copy number variation1nstd102humanPathogenic GRCh37 chr3: 33,138,483-33,166,091 , GRCh38 chr3: 33,096,991-33,124,599 CRTAP, GLB1, 2 more genes
    nsv3969871insertion1nstd168human GRCh38 chr3: 33,036,263-33,134,972 , GRCh37.p13 chr3: 33,077,755-33,176,464 GLB1, CRTAP, 3 more genes
    nsv3923656copy number variation1nstd102humanPathogenic GRCh38 chr3: 11,463,328-38,919,543 , NCBI36 chr3: 11,479,802-38,936,038 , GRCh37 chr3: 11,504,802-38,961,034 RN7SL4P, TOP2B, 348 more genes
    nsv3920512copy number variation1nstd102humanPathogenic GRCh37 chr3: 33,103,691-36,870,931 , NCBI36 chr3: 33,078,695-36,845,935 , GRCh38 chr3: 33,062,199-36,829,440 RN7SKP227, RNA5SP128, 33 more genes
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