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Items: 1 to 20 of 36

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4682039copy number variation1nstd102humanPathogenic GRCh37 chr7: 66,094,032-66,105,401 , GRCh38.p12 chr7: 66,629,045-66,640,414 KCTD7
    nsv5381724copy number variation1nstd102humanPathogenic GRCh37 chr7: 66,094,052-66,104,219 , GRCh38.p12 chr7: 66,629,065-66,639,232 KCTD7
    nsv3874075copy number variation1nstd102humanPathogenic GRCh38 chr7: 66,638,233-66,639,252 , GRCh37 chr7: 66,103,220-66,104,239 KCTD7
    nsv6312787copy number variation1nstd102humanPathogenic GRCh37 chr7: 66,103,220-66,104,219 , GRCh38.p12 chr7: 66,638,233-66,639,232 KCTD7
    nsv3907180copy number variation1nstd102humanPathogenic GRCh37 chr7: 66,103,208-66,105,624 , GRCh38.p12 chr7: 66,638,221-66,640,637 KCTD7
    nsv3872755copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 66,098,242-66,098,451 , GRCh38 chr7: 66,633,255-66,633,464 KCTD7
    nsv6312413copy number variation1nstd102humanLikely benign GRCh37 chr7: 66,098,432-66,108,217 , GRCh38.p12 chr7: 66,633,445-66,643,230 KCTD7
    nsv3884151copy number variation1nstd102humanLikely benign GRCh37 chr7: 66,103,220-66,105,401 , GRCh38 chr7: 66,638,233-66,640,414 KCTD7
    nsv5980434copy number variation1nstd102humanLikely benign GRCh37 chr7: 66,103,230-66,104,219 , GRCh38.p12 chr7: 66,638,243-66,639,232 KCTD7
    nsv4452241copy number variation1nstd102humanUncertain significance GRCh38 chr7: 66,629,045-66,640,414 , GRCh37 chr7: 66,094,032-66,105,401 KCTD7
    nsv7098130copy number variation1nstd102humanUncertain significance GRCh37 chr7: 66,094,052-66,103,438 , GRCh38.p12 chr7: 66,629,065-66,638,451 KCTD7
    nsv7097384copy number variation1nstd102humanUncertain significance GRCh37 chr7: 66,094,052-66,094,215 , GRCh38.p12 chr7: 66,629,065-66,629,228 KCTD7
    nsv6636632copy number variation1nstd102humanUncertain significance GRCh37 chr7: 66,085,625-66,210,558 , GRCh38.p12 chr7: 66,620,638-66,745,571 KCTD7, LOC100996437, 1 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 KCTD7, RNU6-438P, 2682 more genes
    nsv3888815copy number variation1nstd102humanPathogenic GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467 KCTD7, LOC107986817, 2014 more genes
    nsv3917508copy number variation1nstd102humanPathogenic GRCh37 chr7: 62,196,742-75,061,986 , GRCh38 chr7: 62,736,364-75,432,710 , NCBI36 chr7: 61,834,177-74,899,922 KCTD7, GTF2IP4, 285 more genes
    nsv3923428copy number variation1nstd102humanPathogenic GRCh38 chr7: 64,657,050-72,243,063 , NCBI36 chr7: 63,754,863-71,345,984 , GRCh37 chr7: 64,117,428-71,708,048 KCTD7, LOC402279, 112 more genes
    nsv3906315copy number variation1nstd102humanPathogenic GRCh37 chr7: 63,583,563-71,047,246 , GRCh38.p12 chr7: 64,123,185-71,582,261 KCTD7, LINC01372, 133 more genes
    nsv3894780copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842 KCTD7, RNU6-565P, 2684 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 KCTD7, RPL23AP51, 2684 more genes
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