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Items: 1 to 20 of 62

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4455084copy number variation1nstd102humanUncertain significance GRCh37 chr10: 19,774,176-22,330,966 , GRCh38.p12 chr10: 19,485,247-22,042,037 LOC105376445, NEBL-AS1, 33 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4179917copy number variation1nstd166human GRCh37.p13 chr10: 22,146,757-22,254,172 , GRCh38.p12 chr10: 21,857,828-21,965,243 RN7SKP37, DNAJC1
    nsv3920796copy number variation1nstd102humanPathogenic NCBI36 chr10: 62,842-35,729,127 , GRCh37.p13 chr10: 72,842-35,689,121 , GRCh38.p12 chr10: 26,906-35,400,193 EPC1-AS1, RNU6-452P, 559 more genes
    nsv3920598copy number variation1nstd102humanBenign NCBI36 chr10: 4,636,926-47,125,152 , GRCh38 chr10: 4,604,734-48,074,662 , GRCh37 chr10: 4,646,926-47,531,169 LOC100420467, LOC105376474, 709 more genes
    nsv3917667copy number variation1nstd102humanPathogenic GRCh37 chr10: 224,406-26,628,907 , GRCh38 chr10: 90,205-26,339,978 , NCBI36 chr10: 126,145-26,668,913 RN7SKP241, DIP2C-AS1, 389 more genes
    nsv3916980copy number variation1nstd102humanUncertain significance GRCh37 chr10: 21,253,899-22,338,483 , GRCh38 chr10: 20,964,970-22,049,554 , NCBI36 chr10: 21,293,905-22,378,489 RNU6-1141P, RN7SKP219, 19 more genes
    nsv3911634copy number variation1nstd102humanLikely pathogenic NCBI36 chr10: 19,417,096-33,061,227 , GRCh37 chr10: 19,377,090-33,021,221 , GRCh38 chr10: 19,088,161-32,732,293 BMI1, CCND3P1, 221 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 LOC100419870, LOC102724439, 2105 more genes
    nsv3904390copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,026-50,961,640 , GRCh38.p12 chr10: 54,086-49,753,594 LINC00700, LINC02881, 806 more genes
    nsv3903440copy number variation1nstd102humanUncertain significance GRCh37 chr10: 21,881,989-23,129,991 , GRCh38.p12 chr10: 21,593,060-22,841,062 TRN-GTT2-3, DNAJC1, 22 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 ANXA11, EDRF1-DT, 2085 more genes
    nsv3891958copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414 TUBB8, PPP2R2D, 2085 more genes
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 AGAP14P, LOC100505502, 2097 more genes
    nsv3169255copy number variation1nstd158human GRCh37 chr10: 6,588,549-24,063,075 , GRCh38.p12 chr10: 6,546,587-23,774,146 , ATP5F1C, 247 more genes
    nsv3168485inversion1nstd158human GRCh37 chr10: 8,177,319-27,193,925 , GRCh38.p12 chr10: 8,135,356-26,904,996 , BMI1, 257 more genes
    nsv2784244copy number variation1nstd132human NCBI36 chr10: 21,909,174-22,434,029 , GRCh37.p13 chr10: 21,869,168-22,394,023 , GRCh38.p12 chr10: 21,580,239-22,105,094 MLLT10, DNAJC1, 6 more genes
    nsv2782928copy number variation1nstd132human NCBI36 chr10: 21,918,150-22,416,845 , GRCh37.p13 chr10: 21,878,144-22,376,839 , GRCh38.p12 chr10: 21,589,215-22,087,910 MLLT10, DNAJC1, 5 more genes
    nsv2747311copy number variation3nstd130human NCBI36 chr10: 22,187,338-22,283,078 , GRCh37.p13 chr10: 22,147,332-22,243,072 , GRCh38.p12 chr10: 21,858,403-21,954,143 RN7SKP37, DNAJC1
    nsv2730882copy number variation3nstd130human NCBI36 chr10: 22,152,762-22,283,078 , GRCh37.p13 chr10: 22,112,756-22,243,072 , GRCh38.p12 chr10: 21,823,827-21,954,143 DNAJC1, RN7SKP37
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