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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5902965copy number variation1nstd209human GRCh38 chr3: 77,088,725-77,090,322 , GRCh37.p13 chr3: 77,137,876-77,139,473 ROBO2, RNU6-386P
    nsv5836500copy number variation2nstd209human GRCh38 chr3: 77,088,678-77,090,727 , GRCh37.p13 chr3: 77,137,829-77,139,878 RNU6-386P, ROBO2
    nsv5033386inversion1nstd200human GRCh38 chr3: 66,830,019-82,426,887 , GRCh37.p13 chr3: 66,880,443-82,476,038 , HNRNPA3P6, 150 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
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4454606copy number variation1nstd102humanUncertain significance GRCh37 chr3: 77,002,316-77,751,414 , GRCh38.p12 chr3: 76,953,165-77,702,263 ROBO2, VDAC1P7, 1 more genes
    nsv3923231copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 76,896,101-89,814,775 , GRCh37 chr3: 76,813,411-89,732,085 , GRCh38 chr3: 76,764,260-89,682,935 EPHA3, GBE1, 80 more genes
    nsv3922768copy number variation1nstd102humanPathogenic GRCh37 chr3: 64,746,924-78,459,248 , GRCh38 chr3: 64,761,248-78,410,098 , NCBI36 chr3: 64,721,964-78,541,938 RNU6-557P, LOC105377160, 147 more genes
    nsv3916669copy number variation1nstd102humanPathogenic NCBI36 chr3: 74,781,223-89,627,521 , GRCh37 chr3: 74,698,533-89,544,831 , GRCh38 chr3: 74,649,382-89,495,681 LOC105377187, LOC101927374, 109 more genes
    nsv3916461copy number variation1nstd102humanPathogenic GRCh37 chr3: 57,174,452-90,309,110 , NCBI36 chr3: 57,149,492-90,391,800 , GRCh38 chr3: 57,140,424-90,259,960 LOC105377171, HNRNPA3P6, 323 more genes
    nsv3911768copy number variation1nstd102humanPathogenic NCBI36 chr3: 73,956,712-90,585,539 , GRCh37 chr3: 73,874,022-90,502,849 , GRCh38 chr3: 73,824,871-90,453,699 RN7SKP284, OR7E121P, 122 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
    nsv3881375copy number variation1nstd102humanUncertain significance GRCh37 chr3: 76,240,301-79,418,897 , GRCh38.p12 chr3: 76,191,150-79,369,747 LINC02077, RNU6-386P, 13 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 RPL23AP49, DLEC1, 2875 more genes
    nsv3123799copy number variation1nstd151human GRCh37 chr3: 77,089,934-79,174,692 , GRCh38.p12 chr3: 77,040,783-79,125,542 MRPS17P3, VDAC1P7, 11 more genes
    nsv2182410short tandem repeat9nstd128human GRCh37 chr3: 77,141,132-77,141,178 , GRCh38.p12 chr3: 77,091,981-77,092,027 ROBO2, RNU6-386P
    nsv1194883copy number variation1nstd113human NCBI36 chr3: 76,485,892-79,401,678 , GRCh37.p13 chr3: 76,403,202-79,318,988 , GRCh38.p12 chr3: 76,354,051-79,269,838 , LOC102724949, 14 more genes
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