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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097061copy number variation1nstd102humanPathogenic GRCh37 chr6: 47,471,016-47,471,176 , GRCh38.p12 chr6: 47,503,280-47,503,440 CD2AP
    nsv7058001inversion1nstd229human GRCh38 chr6: 47,441,459-48,144,831 , GRCh37.p13 chr6: 47,409,195-48,112,567 ADGRF2, RPL27AP7, 9 more genes
    nsv7047571inversion1nstd229human GRCh38 chr6: 47,471,816-49,526,857 , GRCh37.p13 chr6: 47,439,552-49,494,570 MMUT, RN7SKP116, 19 more genes
    nsv6798040copy number variation1nstd229human GRCh38 chr6: 47,597,101-47,599,200 , GRCh37.p13 chr6: 47,564,837-47,566,936 LOC100421517, CD2AP
    nsv6797573copy number variation1nstd229human GRCh38 chr6: 47,598,901-47,608,400 , GRCh37.p13 chr6: 47,566,637-47,576,136 CD2AP
    nsv6796992copy number variation1nstd229human GRCh38 chr6: 47,583,320-47,603,359 , GRCh37.p13 chr6: 47,551,056-47,571,095 CD2AP, LOC100421517
    nsv6796341copy number variation1nstd229human GRCh38 chr6: 47,599,001-47,602,500 , GRCh37.p13 chr6: 47,566,737-47,570,236 CD2AP
    nsv6792123copy number variation1nstd229human GRCh38 chr6: 47,597,001-47,599,300 , GRCh37.p13 chr6: 47,564,737-47,567,036 LOC100421517, CD2AP
    nsv6789616copy number variation1nstd229human GRCh38 chr6: 47,486,561-47,493,406 , GRCh37.p13 chr6: 47,454,297-47,461,142 CD2AP
    nsv6789166copy number variation1nstd229human GRCh38 chr6: 47,598,213-47,619,770 , GRCh37.p13 chr6: 47,565,949-47,587,506 LOC100421517, CD2AP
    nsv6788345copy number variation1nstd229human GRCh38 chr6: 47,607,119-47,607,138 , GRCh37.p13 chr6: 47,574,855-47,574,874 CD2AP
    nsv6786052copy number variation1nstd229human GRCh38 chr6: 47,525,876-47,526,006 , GRCh37.p13 chr6: 47,493,612-47,493,742 CD2AP
    nsv6785082copy number variation1nstd229human GRCh38 chr6: 47,599,201-47,613,800 , GRCh37.p13 chr6: 47,566,937-47,581,536 CD2AP
    nsv6784658copy number variation1nstd229human GRCh38 chr6: 47,583,277-47,586,537 , GRCh37.p13 chr6: 47,551,013-47,554,273 CD2AP
    nsv6784115copy number variation1nstd229human GRCh38 chr6: 47,598,801-47,635,900 , GRCh37.p13 chr6: 47,566,537-47,603,636 CD2AP
    nsv6782987copy number variation1nstd229human GRCh38 chr6: 47,598,701-47,607,700 , GRCh37.p13 chr6: 47,566,437-47,575,436 CD2AP
    nsv6782386copy number variation1nstd229human GRCh38 chr6: 47,547,718-47,553,415 , GRCh37.p13 chr6: 47,515,454-47,521,151 CD2AP
    nsv6782000copy number variation1nstd229human GRCh38 chr6: 47,507,778-47,508,292 , GRCh37.p13 chr6: 47,475,514-47,476,028 CD2AP
    nsv6781300copy number variation1nstd229human GRCh38 chr6: 47,586,001-47,596,700 , GRCh37.p13 chr6: 47,553,737-47,564,436 CD2AP, LOC100421517
    nsv6781076copy number variation1nstd229human GRCh38 chr6: 47,491,801-47,515,500 , GRCh37.p13 chr6: 47,459,537-47,483,236 CD2AP
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