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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095130copy number variation1nstd102humanUncertain significance GRCh37 chr17: 1,173,858-1,174,565 , GRCh38.p12 chr17: 1,270,564-1,271,271 BHLHA9
    nsv6315029copy number variation1nstd102humanPathogenic GRCh37 chr17: 1,164,471-1,239,336 , GRCh38.p12 chr17: 1,261,177-1,336,042 , GRCh38.p12 chr17|NT_187613.1: 238,839-278,068 BHLHA9, TRARG1
    nsv3901480copy number variation1nstd102humanUncertain significance GRCh37 chr17: 1,147,903-1,234,046 , GRCh38.p12 chr17: 1,244,609-1,330,752 BHLHA9, TRARG1
    nsv4436572copy number variation1nstd102humanPathogenic GRCh37 chr17: 1,130,776-1,361,490 , GRCh38 chr17: 1,227,482-1,458,196 BHLHA9, ABR, 3 more genes
    nsv4349306copy number variation1nstd102humanPathogenic GRCh37 chr17: 1,084,016-1,278,527 , GRCh38.p12 chr17: 1,180,722-1,375,233 BHLHA9, ABR, 3 more genes
    nsv6315043copy number variation1nstd102humanPathogenic GRCh37 chr17: 1,124,394-1,186,190 , GRCh38.p12 chr17: 1,221,100-1,282,896 BHLHA9, ABR, 1 more genes
    nsv3899810copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 1,165,433-1,277,056 , GRCh38.p12 chr17: 1,262,139-1,373,762 , GRCh38.p12 chr17|NT_187613.1: 238,839-315,788 BHLHA9, YWHAE, 1 more genes
    nsv6637865copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 1,070,609-1,281,546 , GRCh38.p12 chr17: 1,167,315-1,378,252 , GRCh38.p12 chr17|NT_187613.1: 211,515-320,278 BHLHA9, ABR, 3 more genes
    nsv4729881copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 1,121,817-1,277,056 , GRCh38.p12 chr17: 1,218,523-1,373,762 BHLHA9, ABR, 2 more genes
    nsv3918715copy number variation1nstd102humanLikely benign NCBI36 chr17: 1,008,184-1,223,994 , GRCh37 chr17: 1,061,434-1,277,244 , GRCh38 chr17: 1,158,140-1,373,950 BHLHA9, ABR-AS1, 3 more genes
    nsv3901387copy number variation1nstd102humanBenign GRCh37 chr17: 1,068,393-1,209,162 , GRCh38.p12 chr17: 1,165,099-1,305,868 BHLHA9, TRARG1, 2 more genes
    nsv3872991copy number variation1nstd102humannot provided GRCh37 chr17: 1,116,991-1,239,946 , GRCh38 chr17: 1,213,697-1,336,652 BHLHA9, ABR, 1 more genes
    nsv3891799copy number variation1nstd102humanUncertain significance GRCh37 chr17: 1,061,693-1,264,288 , GRCh38.p12 chr17: 1,158,399-1,360,994 BHLHA9, ABR, 3 more genes
    nsv3902017copy number variation1nstd102humanUncertain significance GRCh37 chr17: 1,061,693-1,256,253 , GRCh38.p12 chr17: 1,158,399-1,352,959 BHLHA9, ABR-AS1, 3 more genes
    nsv4457690copy number variation1nstd102humanUncertain significance GRCh37 chr17: 1,103,339-1,277,056 , GRCh38.p12 chr17: 1,200,045-1,373,762 BHLHA9, ABR, 2 more genes
    nsv3900491copy number variation1nstd102humanUncertain significance GRCh37 chr17: 1,121,817-1,270,757 , GRCh38.p12 chr17: 1,218,523-1,367,463 BHLHA9, ABR, 2 more genes
    nsv4457868copy number variation1nstd102humanUncertain significance GRCh37 chr17: 1,124,664-1,264,198 , GRCh38.p12 chr17: 1,221,370-1,360,904 BHLHA9, YWHAE, 2 more genes
    esv3648801copy number variation1estd216humannot provided GRCh37 chr17: 1,116,991-1,239,946 , GRCh38.p12 chr17: 1,213,697-1,336,652 BHLHA9, ABR, 2 more genes
    nsv3914259copy number variation1nstd102humanPathogenic NCBI36 chr17: 1,077,526-1,356,592 , GRCh37 chr17: 1,130,776-1,409,842 , GRCh38 chr17: 1,227,482-1,506,548 BHLHA9, ABR, 6 more genes
    nsv3913013copy number variation1nstd102humanPathogenic GRCh38 chr17: 162,016-7,697,012 , GRCh37 chr17: 45,835-7,600,330 , NCBI36 chr17: 11,807-7,541,055 BHLHA9, RPS4XP17, 289 more genes
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