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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980034inversion1nstd209human GRCh38 chr3: 83,154,897-85,212,825 , GRCh37.p13 chr3: 83,204,048-85,261,975 CADM2, LINC00971, 11 more genes
    nsv4929026copy number variation1nstd200human GRCh38 chr3: 84,707,233-85,329,501 , GRCh37.p13 chr3: 84,756,384-85,378,651 LOC105377193, CADM2, 3 more genes
    nsv4927594copy number variation1nstd200human GRCh38 chr3: 84,871,098-84,990,486 , GRCh37.p13 chr3: 84,920,249-85,039,637 CADM2, LOC105377193, 1 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4728420copy number variation1nstd102humanUncertain significance GRCh37 chr3: 80,873,527-85,127,795 , GRCh38.p12 chr3: 80,824,376-85,078,644 LOC105377193, SRRM1P2, 21 more genes
    nsv4674346copy number variation1nstd102humanUncertain significance GRCh37 chr3: 83,681,388-85,570,265 , GRCh38.p12 chr3: 83,632,237-85,521,115 LOC105377193, SRRM1P2, 9 more genes
    nsv4568251inversion1nstd166human GRCh37.p13 chr3: 81,845,861-90,137,796 , GRCh38.p12 chr3: 81,796,710-90,088,646 POU1F1, CHMP2B, 54 more genes
    nsv4451776copy number variation1nstd102humanUncertain significance GRCh37 chr3: 84,757,732-85,375,831 , GRCh38.p12 chr3: 84,708,581-85,326,681 LINC00971, SNORA95, 3 more genes
    nsv3960295insertion1nstd168human GRCh38 chr3: 84,855,883-84,914,137 , GRCh37.p13 chr3: 84,905,034-84,963,288 LINC00971, LINC02025, 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
    nsv3921691copy number variation1nstd102humanPathogenic NCBI36 chr3: 81,636,154-85,259,739 , GRCh38 chr3: 81,504,313-85,127,899 , GRCh37 chr3: 81,553,464-85,177,049 LOC105377187, CADM2, 19 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
    nsv3912472copy number variation1nstd102humanUncertain significance GRCh38 chr3: 80,320,584-87,468,216 , GRCh37 chr3: 80,369,734-87,517,366 , NCBI36 chr3: 80,452,424-87,600,056 LINC02070, LOC105377181, 41 more genes
    nsv3912034copy number variation1nstd102humanPathogenic GRCh38 chr3: 82,912,987-90,179,222 , GRCh37 chr3: 82,962,138-90,228,372 , NCBI36 chr3: 83,044,828-90,311,062 MTATP6P6, SNORA95, 49 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
    nsv3889683copy number variation1nstd102humanUncertain significance GRCh37 chr3: 81,307,181-86,030,178 , GRCh38.p12 chr3: 81,258,030-85,981,028 LOC105377183, SETP6, 21 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
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 RPL23AP49, DLEC1, 2875 more genes
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