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Items: 1 to 20 of 177

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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
    nsv7054319inversion1nstd229human GRCh38 chr4: 40,437,339-43,087,585 , GRCh37.p13 chr4: 40,439,356-43,089,602 RN7SKP82, RPS7P7, 33 more genes
    nsv6733879copy number variation1nstd229human GRCh38 chr4: 42,107,933-42,110,897 , GRCh37.p13 chr4: 42,109,950-42,112,914 BEND4
    nsv6729390copy number variation1nstd229human GRCh38 chr4: 42,140,236-42,140,463 , GRCh37.p13 chr4: 42,142,253-42,142,480 BEND4
    nsv6719906copy number variation1nstd229human GRCh38 chr4: 42,121,070-42,121,225 , GRCh37.p13 chr4: 42,123,087-42,123,242 BEND4
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6561211inversion1nstd223human GRCh38 chr4: 42,142,014-42,142,524 , GRCh37.p13 chr4: 42,144,031-42,144,541 BEND4
    nsv6558368inversion1nstd223human GRCh38 chr4: 42,117,983-42,118,227 , GRCh37.p13 chr4: 42,120,000-42,120,244 BEND4
    nsv6391720copy number variation1nstd223human GRCh38 chr4: 42,140,235-42,140,463 , GRCh37.p13 chr4: 42,142,252-42,142,480 BEND4
    nsv6387702copy number variation1nstd223human GRCh38 chr4: 42,133,672-42,135,589 , GRCh37.p13 chr4: 42,135,689-42,137,606 BEND4
    nsv6384949copy number variation1nstd223human GRCh38 chr4: 42,138,034-42,138,542 , GRCh37.p13 chr4: 42,140,051-42,140,559 BEND4
    nsv6315440copy number variation1nstd102humanPathogenic GRCh37 chr4: 114,784-47,569,569 , GRCh38.p12 chr4: 114,902-47,567,552 FAM86KP, ENPP7P11, 631 more genes
    nsv6299490copy number variation1nstd186human GRCh37 chr4: 42,121,555-42,121,711 , GRCh38.p12 chr4: 42,119,538-42,119,694 BEND4
    nsv6135340copy number variation1nstd213human GRCh37 chr4: 42,040,000-42,610,001 , GRCh38.p12 chr4: 42,037,983-42,607,984 ATP8A1, SLC30A9, 5 more genes
    nsv6135262copy number variation1nstd213human GRCh37 chr4: 42,089,111-42,216,858 , GRCh38.p12 chr4: 42,087,094-42,214,841 SLC30A9, BEND4
    nsv5997208copy number variation1nstd212human GRCh38 chr4: 42,136,266-42,136,385 , GRCh37.p13 chr4: 42,138,283-42,138,402 BEND4
    nsv5610235insertion1nstd207human GRCh38 chr4: 42,110,060-42,110,060 , GRCh37.p13 chr4: 42,112,077-42,112,077 BEND4
    nsv5459038copy number variation1nstd206human GRCh38 chr4: 42,119,538-42,119,694 , GRCh37.p13 chr4: 42,121,555-42,121,711 BEND4
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