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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3907997copy number variation1nstd102humanBenign GRCh37 chrX: 2,118,389-2,289,645 , NCBI36 chrX: 2,128,389-2,299,645 , GRCh38 chrX: 2,200,415-2,371,604 DHRSX
    nsv3908338copy number variation1nstd102humanLikely benign GRCh38 chrX: 2,295,867-2,345,083 , GRCh37 chrX: 2,213,908-2,263,124 , NCBI36 chrX: 2,223,908-2,273,124 DHRSX
    nsv4728300copy number variation1nstd102humanLikely benign GRCh37 chrX: 2,019,137-2,361,706 , GRCh38.p12 chrX: 1,900,244-2,443,665 DHRSX
    nsv3877593copy number variation1nstd102humanBenign GRCh37 chrX: 2,066,618-2,361,399 , GRCh38.p12 chrX: 1,947,725-2,443,358 DHRSX
    nsv3886269copy number variation1nstd102humanLikely benign GRCh37 chrX: 2,059,627-2,314,248 , GRCh38.p12 chrX: 1,940,734-2,396,207 DHRSX
    nsv3896615copy number variation1nstd102humanLikely benign GRCh38 chrX: 1,898,416-2,326,714 , GRCh37 chrX: 2,017,309-2,244,755 , NCBI36 chrX: 1,977,309-2,254,755 DHRSX
    nsv3876576copy number variation1nstd102humanBenign GRCh37 chrX: 2,066,618-2,272,030 , GRCh38.p12 chrX: 1,947,725-2,353,989 DHRSX
    nsv3882360copy number variation1nstd102humanLikely benign GRCh37 chrX: 2,052,936-2,170,438 , GRCh38.p12 chrX: 1,934,043-2,252,397 DHRSX
    nsv3898275copy number variation1nstd102humanBenign GRCh38 chrX: 1,947,725-2,248,818 , GRCh37 chrX: 2,066,618-2,166,859 , NCBI36 chrX: 2,026,618-2,176,859 DHRSX
    nsv3889344copy number variation1nstd102humanLikely benign GRCh37 chrX: 2,066,618-2,166,859 , GRCh38.p12 chrX: 1,947,725-2,248,818 DHRSX
    nsv4674331copy number variation1nstd102humanLikely benign GRCh37 chrX: 2,124,302-2,400,774 , GRCh38.p12 chrX: 2,206,295-2,482,733 DHRSX
    nsv3897494copy number variation1nstd102humanBenign NCBI36 chrY: 2,271,474-2,371,399 , GRCh37 chrY: 2,211,474-2,311,399 , GRCh38 chrY: 2,343,433-2,443,358 DHRSX
    nsv3921876copy number variation1nstd102humanUncertain significance NCBI36 chrX: 2,236,551-2,314,656 , GRCh37.p13 chrX: 2,226,551-2,304,656 , GRCh38.p12 chrX: 2,308,510-2,386,615 DHRSX
    nsv3915685copy number variation1nstd102humanUncertain significance NCBI36 chrY: 2,236,551-2,314,572 , GRCh37.p13 chrY: 2,176,551-2,254,572 , GRCh38.p12 chrY: 2,308,510-2,386,531 DHRSX
    nsv3917013copy number variation1nstd102humanUncertain significance NCBI36 chrY: 2,017,128-2,290,197 , GRCh37.p13 chrY: 2,007,128-2,230,197 , GRCh38.p12 chrY: 1,938,235-2,362,156 DHRSX
    nsv3924119copy number variation1nstd102humanUncertain significance NCBI36 chrX: 2,017,128-2,265,330 , GRCh37.p13 chrX: 2,057,128-2,255,330 , GRCh38.p12 chrX: 1,938,235-2,337,289 DHRSX
    nsv3920663copy number variation1nstd102humanUncertain significance NCBI36 chrX: 2,273,124-2,374,801 , GRCh37.p13 chrX: 2,263,124-2,364,801 , GRCh38.p12 chrX: 2,345,083-2,446,760 DHRSX
    nsv3906405copy number variation1nstd102humanPathogenic GRCh38 chrY: 2,210,832-2,525,377 , GRCh37 chrY: 2,078,852-2,393,418 , NCBI36 chrY: 2,138,852-2,453,418 DHRSX, ZBED1
    nsv3877177copy number variation1nstd102humanBenign GRCh37 chrX: 1,942,205-2,272,030 , GRCh38.p12 chrX: 1,823,312-2,353,989 DHRSX, LOC107985677
    nsv3920057copy number variation1nstd102humanUncertain significance NCBI36 chrX: 1,924,166-2,403,999 , GRCh37.p13 chrX: 1,964,166-2,393,999 , GRCh38.p12 chrX: 1,845,273-2,475,958 DHRSX, LOC107985677
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