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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
    nsv3908359copy number variation1nstd102humanLikely pathogenic NCBI36 chrX: 38,376,483-38,442,479 , GRCh37 chrX: 38,491,539-38,557,535 , GRCh38 chrX: 38,632,286-38,698,281 TSPAN7
    nsv3874968copy number variation1nstd102humanLikely benign GRCh37 chrX: 38,480,090-38,639,494 , GRCh38.p12 chrX: 38,620,837-38,780,241 TSPAN7
    nsv3901663copy number variation1nstd102humanLikely benign GRCh38 chrX: 38,617,950-38,775,361 , NCBI36 chrX: 38,362,147-38,519,558 , GRCh37 chrX: 38,477,203-38,634,614 TSPAN7
    nsv3874731copy number variation2nstd102humannot provided, Likely benign GRCh37 chrX: 38,480,090-38,634,614 , GRCh38.p12 chrX: 38,620,837-38,775,361 TSPAN7
    nsv3874235copy number variation1nstd102humanLikely benign GRCh37 chrX: 38,486,619-38,628,557 , GRCh38.p12 chrX: 38,627,366-38,769,304 TSPAN7
    nsv3879415copy number variation1nstd102humanBenign GRCh37 chrX: 38,486,922-38,628,467 , GRCh38.p12 chrX: 38,627,669-38,769,214 TSPAN7
    nsv3880734copy number variation1nstd102humanBenign GRCh37 chrX: 38,490,102-38,628,467 , GRCh38.p12 chrX: 38,630,849-38,769,214 TSPAN7
    nsv3870939copy number variation1nstd102humanLikely benign GRCh37 chrX: 38,491,539-38,628,756 , GRCh38.p12 chrX: 38,632,286-38,769,503 TSPAN7
    nsv3877659copy number variation1nstd102humanBenign GRCh37 chrX: 38,490,844-38,624,791 , GRCh38.p12 chrX: 38,631,591-38,765,538 TSPAN7
    nsv3886076copy number variation1nstd102humanBenign GRCh37 chrX: 38,490,844-38,577,270 , GRCh38.p12 chrX: 38,631,591-38,718,016 TSPAN7
    nsv3899529copy number variation1nstd102humanLikely benign GRCh37 chrX: 38,488,591-38,547,960 , GRCh38 chrX: 38,629,338-38,688,706 , NCBI36 chrX: 38,373,535-38,432,904 TSPAN7
    nsv3892362copy number variation2nstd102humanBenign GRCh38 chrX: 38,629,364-38,688,697 , GRCh37 chrX: 38,488,617-38,547,951 , NCBI36 chrX: 38,373,561-38,432,895 TSPAN7
    nsv3917431copy number variation1nstd102humanUncertain significance NCBI36 chrX: 38,369,316-38,529,542 , GRCh37.p13 chrX: 38,484,372-38,644,598 , GRCh38.p12 chrX: 38,625,119-38,785,345 TSPAN7
    nsv3886142copy number variation1nstd102humanUncertain significance GRCh37 chrX: 38,480,079-38,634,706 , GRCh38.p12 chrX: 38,620,826-38,775,453 TSPAN7
    nsv3900583copy number variation1nstd102humanUncertain significance NCBI36 chrX: 38,365,023-38,519,558 , GRCh38 chrX: 38,620,826-38,775,361 , GRCh37 chrX: 38,480,079-38,634,614 TSPAN7
    nsv3876748copy number variation1nstd102humanUncertain significance GRCh37 chrX: 38,480,079-38,634,614 , GRCh38.p12 chrX: 38,620,826-38,775,361 TSPAN7
    nsv4449907copy number variation1nstd102humanUncertain significance GRCh37 chrX: 38,476,857-38,629,433 , GRCh38.p12 chrX: 38,617,604-38,770,180 TSPAN7
    nsv3882748copy number variation1nstd102humanUncertain significance GRCh37 chrX: 38,480,090-38,628,557 , GRCh38.p12 chrX: 38,620,837-38,769,304 TSPAN7
    nsv3889618copy number variation2nstd102humanUncertain significance GRCh37 chrX: 38,486,618-38,634,614 , GRCh38.p12 chrX: 38,627,365-38,775,361 TSPAN7
    nsv3874060copy number variation1nstd102humanUncertain significance GRCh37 chrX: 38,486,799-38,634,706 , GRCh38.p12 chrX: 38,627,546-38,775,453 TSPAN7
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