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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2666739copy number variation325estd199human GRCh37 chr1: 207,699,545-207,737,892 , GRCh38.p12 chr1: 207,526,200-207,564,547 CR1
    esv2668226copy number variation311estd199human GRCh37 chr3: 129,763,245-129,799,692 , GRCh38.p12 chr3: 130,044,402-130,080,849 ALG1L2
    esv2673583copy number variation519estd199human GRCh37 chr20: 1,560,991-1,594,041 , GRCh38.p12 chr20: 1,580,345-1,613,395 SIRPB1
    esv2674493copy number variation111estd199human GRCh37 chr1: 169,225,645-169,243,192 , GRCh38.p12 chr1: 169,256,407-169,273,954 NME7
    esv2662901copy number variation324estd199human GRCh37 chr9: 41,969,445-41,984,392 , GRCh38.p12 chr9: 39,824,427-39,839,374 FGF7P3
    esv2673726copy number variation33estd199human GRCh37 chr7: 100,327,145-100,340,992 , GRCh38.p12 chr7: 100,729,522-100,743,369 ZAN
    esv2656701copy number variation437estd199human GRCh37 chr16: 78,371,638-78,384,898 , GRCh38.p12 chr16: 78,337,741-78,351,001 WWOX
    esv2675866copy number variation315estd199human GRCh37 chr9: 113,024,576-113,037,093 , GRCh38.p12 chr9: 110,262,296-110,274,813 LOC107987114
    esv2664803copy number variation436estd199human GRCh37 chr15: 76,884,596-76,896,938 , GRCh38.p12 chr15: 76,592,255-76,604,597 SCAPER
    esv2678677copy number variation179estd199human GRCh37 chr15: 76,884,295-76,895,742 , GRCh38.p12 chr15: 76,591,954-76,603,401 SCAPER
    esv2673551copy number variation872estd199human GRCh37 chr3: 192,875,329-192,885,405 , GRCh38.p12 chr3: 193,157,540-193,167,616 VEZF1P1
    esv2678766copy number variation61estd199human GRCh37 chr6: 81,283,718-81,293,577 , GRCh38.p12 chr6: 80,574,001-80,583,860 LOC112267962
    esv2657260copy number variation826estd199human GRCh37 chr2: 87,730,745-87,740,792 , GRCh38.p12 chr2: 87,431,226-87,441,083 LINC01943
    esv2662536copy number variation311estd199human GRCh37 chr6: 72,863,851-72,873,540 , GRCh38.p12 chr6: 72,154,148-72,163,837 RIMS1
    esv2661768copy number variation445estd199human GRCh37 chr5: 12,811,019-12,820,535 , GRCh38.p12 chr5: 12,810,907-12,820,423 LOC105374657
    esv2657410copy number variation26estd199human GRCh37 chr6: 19,041,045-19,050,292 , GRCh38.p12 chr6: 19,040,814-19,050,061 LOC105374958
    esv2673043copy number variation328estd199human GRCh37 chr14: 80,106,288-80,115,049 , GRCh38.p12 chr14: 79,639,945-79,648,706 NRXN3
    esv2657498copy number variation116estd199human GRCh37 chr4: 21,160,045-21,167,592 , GRCh38.p12 chr4: 21,158,422-21,165,969 KCNIP4
    esv2664776copy number variation250estd199human GRCh37 chr3: 191,064,685-191,071,667 , GRCh38.p12 chr3: 191,346,896-191,353,878 CCDC50
    esv2671123copy number variation287estd199human GRCh37 chr4: 107,056,578-107,063,364 , GRCh38.p12 chr4: 106,135,421-106,142,207 TBCK
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