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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7143863insertion1nstd232human GRCh37.p13 chr4: 17,827,184-17,827,184 , GRCh38.p12 chr4: 17,825,561-17,825,561 NCAPG
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    nsv7098818copy number variation1nstd102humanPathogenic GRCh38 chr4: 11,399,082-38,137,335 , GRCh37.p13 chr4: 11,400,706-38,138,956 LOC105374542, PPARGC1A, 232 more genes
    nsv7053890inversion1nstd229human GRCh38 chr4: 16,156,227-18,504,313 , GRCh37.p13 chr4: 16,157,850-18,505,936 TAPT1, NCAPG, 26 more genes
    nsv7047237inversion1nstd229human GRCh38 chr4: 15,975,453-25,472,708 , GRCh37.p13 chr4: 15,977,076-25,474,330 LOC107986219, LOC102723675, 78 more genes
    nsv7044499inversion1nstd229human GRCh38 chr4: 16,435,218-18,199,516 , GRCh37.p13 chr4: 16,436,841-18,201,139 NACAP5, NCAPG, 19 more genes
    nsv6735021copy number variation1nstd229human GRCh38 chr4: 17,675,601-17,836,800 , GRCh37.p13 chr4: 17,677,224-17,838,423 FAM184B, NCAPG, 1 more genes
    nsv6728701copy number variation1nstd229human GRCh38 chr4: 17,375,401-17,812,000 , GRCh37.p13 chr4: 17,377,024-17,813,623 DCAF16, NACAP5, 7 more genes
    nsv6719814copy number variation1nstd229human GRCh38 chr4: 17,826,064-17,826,432 , GRCh37.p13 chr4: 17,827,687-17,828,055 NCAPG
    nsv6637075copy number variation1nstd102humanUncertain significance GRCh37 chr4: 16,249,194-24,864,955 , GRCh38.p12 chr4: 16,247,571-24,863,333 LOC107986262, QDPR, 63 more genes
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6570681inversion1nstd223human GRCh38 chr4: 16,156,227-18,504,312 , GRCh37.p13 chr4: 16,157,850-18,505,935 NCAPG, LOC107986219, 26 more genes
    nsv6566784inversion1nstd223human GRCh38 chr4: 17,820,673-17,821,485 , GRCh37.p13 chr4: 17,822,296-17,823,108 NCAPG
    nsv6375125copy number variation1nstd223human GRCh38 chr4: 17,838,847-17,839,363 , GRCh37.p13 chr4: 17,840,470-17,840,986 LCORL, NCAPG
    nsv6363629copy number variation1nstd223human GRCh38 chr4: 17,840,001-17,842,200 , GRCh37.p13 chr4: 17,841,624-17,843,823 LCORL, NCAPG
    nsv6362762copy number variation1nstd223human GRCh38 chr4: 17,820,892-17,822,785 , GRCh37.p13 chr4: 17,822,515-17,824,408 NCAPG
    nsv6362254copy number variation1nstd223human GRCh38 chr4: 17,003,809-24,506,634 , GRCh37.p13 chr4: 17,005,432-24,508,257 CLRN2, LOC107986220, 48 more genes
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