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Items: 1 to 20 of 314

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098452copy number variation1nstd102humanUncertain significance GRCh37 chr9: 27,047,252-27,573,526 , GRCh38.p12 chr9: 27,047,254-27,573,528 LINC00032, RPL36AP34, 7 more genes
    nsv7063062inversion1nstd229human GRCh38 chr9: 22,592,329-32,576,343 , GRCh37.p13 chr9: 22,592,328-32,576,341 HSPA8P17, RMRPP5, 81 more genes
    nsv7058506inversion1nstd229human GRCh38 chr9: 27,557,581-27,557,688 , GRCh37.p13 chr9: 27,557,579-27,557,686 C9orf72
    nsv6875942copy number variation1nstd229human GRCh38 chr9: 24,741,564-30,889,392 , GRCh37.p13 chr9: 24,741,562-30,889,390 IFNK, LINC01242, 46 more genes
    nsv6870871copy number variation1nstd229human GRCh38 chr9: 27,362,666-27,547,359 , GRCh37.p13 chr9: 27,362,664-27,547,357 C9orf72, IFNK, 1 more genes
    nsv6868209copy number variation1nstd229human GRCh38 chr9: 27,544,532-27,642,363 , GRCh37.p13 chr9: 27,544,530-27,642,361 LOC107987058, CTAGE12P, 1 more genes
    nsv6867999copy number variation1nstd229human GRCh38 chr9: 27,537,744-27,625,646 , GRCh37.p13 chr9: 27,537,742-27,625,644 C9orf72, CTAGE12P
    nsv6865795copy number variation1nstd229human GRCh38 chr9: 27,222,635-27,546,484 , GRCh37.p13 chr9: 27,222,633-27,546,482 C9orf72, LINC00032, 4 more genes
    nsv6865127copy number variation1nstd229human GRCh38 chr9: 27,558,429-27,558,606 , GRCh37.p13 chr9: 27,558,427-27,558,604 C9orf72
    nsv6864275copy number variation1nstd229human GRCh38 chr9: 27,283,384-28,841,224 , GRCh37.p13 chr9: 27,283,382-28,841,222 IFNK, LOC105376003, 10 more genes
    nsv6863572copy number variation1nstd229human GRCh38 chr9: 27,563,010-27,565,871 , GRCh37.p13 chr9: 27,563,008-27,565,869 C9orf72
    nsv6861503copy number variation1nstd229human GRCh38 chr9: 26,680,968-27,607,029 , GRCh37.p13 chr9: 26,680,966-27,607,027 CTAGE12P, LOC105369289, 16 more genes
    nsv6858500copy number variation1nstd229human GRCh38 chr9: 27,291,214-28,145,540 , GRCh37.p13 chr9: 27,291,212-28,145,538 IFNK, LOC107987058, 6 more genes
    nsv6637770copy number variation1nstd102humanUncertain significance GRCh37 chr9: 27,257,570-31,635,608 , GRCh38.p12 chr9: 27,257,572-31,635,610 LOC105376002, CDRT15P5, 32 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6634409copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729 ACO1, PLIN2, 594 more genes
    nsv6633736copy number variation1nstd224human GRCh37 chr9: 27,292,443-28,141,923 , GRCh38.p12 chr9: 27,292,445-28,141,925 EQTN, IFNK, 6 more genes
    nsv6566560inversion1nstd223human GRCh38 chr9: 27,558,530-27,563,285 , GRCh37.p13 chr9: 27,558,528-27,563,283 C9orf72
    nsv6562498inversion1nstd223human GRCh38 chr9: 20,655,689-27,693,631 , GRCh37.p13 chr9: 20,655,688-27,693,629 IFNA7, IFNW1, 92 more genes
    nsv6429817copy number variation1nstd223human GRCh38 chr9: 27,562,506-27,563,142 , GRCh37.p13 chr9: 27,562,504-27,563,140 C9orf72
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