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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3897884copy number variation1nstd102humanBenign GRCh37 chr22: 23,568,858-23,585,132 , GRCh38.p12 chr22: 23,226,671-23,242,945 BCR
    nsv3908147copy number variation1nstd102humanBenign GRCh37 chr22: 23,569,063-23,585,132 , GRCh38.p12 chr22: 23,226,876-23,242,945 BCR
    nsv3909728copy number variation1nstd102humanBenign GRCh37 chr22: 23,576,928-23,587,894 , GRCh38.p12 chr22: 23,234,741-23,245,707 BCR
    nsv3905700copy number variation1nstd102humanBenign GRCh37 chr22: 23,568,858-23,577,294 , GRCh38.p12 chr22: 23,226,671-23,235,107 BCR
    nsv3899097copy number variation1nstd102humanBenign GRCh37 chr9: 133,751,526-133,752,906 , GRCh38.p12 chr9: 130,876,139-130,877,519 ABL1
    nsv3893633copy number variation1nstd102humanBenign GRCh37 chr22: 23,576,928-23,577,722 , GRCh38.p12 chr22: 23,234,741-23,235,535 BCR
    nsv3895346copy number variation1nstd102humanBenign GRCh37 chr22: 23,577,033-23,577,722 , GRCh38.p12 chr22: 23,234,846-23,235,535 BCR
    nsv3906228copy number variation1nstd102humanBenign GRCh37 chr9: 133,752,464-133,752,906 , GRCh38.p12 chr9: 130,877,077-130,877,519 ABL1
    nsv3890770copy number variation1nstd102humanBenign GRCh37 chr22: 23,576,928-23,577,294 , GRCh38.p12 chr22: 23,234,741-23,235,107 BCR
    nsv3891038copy number variation1nstd102humanBenign GRCh37 chr22: 23,576,981-23,577,294 , GRCh38.p12 chr22: 23,234,794-23,235,107 BCR
    nsv3890979copy number variation1nstd102humanUncertain significance GRCh37 chr9: 133,628,752-133,696,938 , GRCh38.p12 chr9: 130,753,365-130,821,551 ABL1
    nsv7098428copy number variation1nstd102humanUncertain significance GRCh37 chr9: 133,755,435-133,761,070 , GRCh38.p12 chr9: 130,880,048-130,885,683 ABL1
    nsv7098062copy number variation1nstd102humanUncertain significance GRCh37 chr9: 133,589,707-133,589,862 , GRCh38.p12 chr9: 130,714,320-130,714,475 ABL1
    nsv3901086copy number variation1nstd102humanBenign GRCh37 chr22: 21,438,417-21,463,730 , GRCh38.p12 chr22: 21,084,128-21,109,441 LOC112268300, BCRP2
    nsv6312846copy number variation1nstd102humanUncertain significance GRCh37 chr9: 133,573,529-133,589,862 , GRCh38.p12 chr9: 130,698,142-130,714,475 ABL1, EXOSC2
    nsv3922346copy number variation1nstd102humanBenign NCBI36 chr22: 19,730,683-19,791,752 , GRCh38 chr22: 21,046,394-21,107,463 , GRCh37 chr22: 21,400,683-21,461,752 LOC112268300, TUBA3GP, 2 more genes
    nsv3892540copy number variation1nstd102humanBenign GRCh37 chr22: 23,497,674-23,542,394 , GRCh38.p12 chr22: 23,155,487-23,200,207 BCR, BCRP8, 2 more genes
    nsv3893695copy number variation1nstd102humanLikely benign GRCh37 chr22: 24,622,697-24,658,565 , GRCh38.p12 chr22: 24,226,729-24,262,597 POM121L9P, GGT5, 2 more genes
    nsv3906510copy number variation1nstd102humanLikely benign GRCh37 chr22: 24,640,758-24,658,665 , GRCh38.p12 chr22: 24,244,790-24,262,697 BCRP1, GGTLC4P, 2 more genes
    nsv3904280copy number variation1nstd102humanBenign/Likely benign GRCh37 chr22: 24,640,758-24,658,565 , GRCh38.p12 chr22: 24,244,790-24,262,597 BCRP1, GGTLC4P, 2 more genes
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