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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3888024copy number variation1nstd102humanBenign GRCh37 chr5: 125,301,304-125,441,148 , GRCh38.p12 chr5: 125,965,611-126,105,455 RPSAP37
    nsv3886992copy number variation1nstd102humanPathogenic GRCh37 chrX: 132,815,787-132,973,332 , GRCh38.p12 chrX: 133,681,759-133,839,305 RPSAP63, GPC3
    nsv1397938copy number variation1nstd102humanPathogenic GRCh37 chrX: 132,834,006-132,986,815 , GRCh38.p12 chrX: 133,699,978-133,852,788 GPC3, RPSAP63
    nsv3887924copy number variation1nstd102humanPathogenic GRCh37 chr1: 236,958,984-237,060,964 , GRCh38 chr1: 236,795,684-236,897,664 RPSAP21, MTR
    nsv6636772copy number variation1nstd102humanPathogenic GRCh37 chrX: 132,879,202-132,956,033 , GRCh38.p12 chrX: 133,745,175-133,822,006 RPSAP63, GPC3
    nsv3170348copy number variation1nstd45humanPathogenic GRCh37 chrX: 53,262,058-53,350,522 , GRCh38.p12 chrX: 53,232,876-53,321,324 IQSEC2, RPSAP62
    nsv3907368copy number variation1nstd102humanBenign GRCh37 chr15: 53,173,116-53,189,197 , GRCh38.p12 chr15: 52,880,919-52,897,000 RPSAP55, LOC107983981
    nsv3902619copy number variation1nstd102humanBenign GRCh37 chr12: 8,895,335-8,898,755 , GRCh38.p12 chr12: 8,742,739-8,746,159 RPSAP51, RIMKLB
    nsv3902851copy number variation1nstd102humanBenign GRCh37 chr15: 53,163,084-53,187,457 , GRCh38.p12 chr15: 52,870,887-52,895,260 RPSAP55, LOC107983981
    nsv5674150copy number variation1nstd102humanLikely benign GRCh37 chrX: 53,349,605-53,350,321 , GRCh38.p12 chrX: 53,320,407-53,321,123 IQSEC2, RPSAP62
    nsv3920245copy number variation1nstd102humanUncertain significance NCBI36 chrX: 86,838,490-86,980,227 , GRCh37.p13 chrX: 86,951,834-87,093,571 , GRCh38.p12 chrX: 87,696,834-87,838,571 RPSAP15, MRPS22P1
    nsv7096034copy number variation1nstd102humanUncertain significance GRCh37 chr1: 236,959,004-237,060,944 , GRCh38.p12 chr1: 236,795,704-236,897,644 RPSAP21, MTR
    nsv3892034copy number variation1nstd102humanPathogenic NCBI36 chrX: 98,153,211-99,451,618 , GRCh37 chrX: 98,266,555-99,564,962 , GRCh38 chrX: 99,011,557-100,309,964 PCDH19, RPSAP8, 3 more genes
    nsv6313035copy number variation1nstd102humanPathogenic GRCh37 chrX: 132,670,132-133,119,496 , GRCh38.p12 chrX: 133,536,104-133,985,469 GPC3, GPC3-AS1, 2 more genes
    nsv4683067copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chrX: 132,670,146-133,119,482 , GRCh38.p12 chrX: 133,536,118-133,985,455 GPC3, RPSAP63, 2 more genes
    nsv6313388copy number variation1nstd102humanPathogenic GRCh37 chrX: 99,398,853-99,802,950 , GRCh38.p12 chrX: 100,143,855-100,547,953 PCDH19, RPSAP8, 1 more genes
    nsv3907906copy number variation1nstd102humanPathogenic NCBI36 chrX: 132,649,003-133,052,166 , GRCh37 chrX: 132,821,337-133,224,500 , GRCh38 chrX: 133,687,309-134,090,471 RPSAP63, GPC3, 1 more genes
    nsv3917735copy number variation1nstd102humanPathogenic GRCh37 chrX: 132,795,738-133,119,496 , GRCh38.p12 chrX: 133,661,710-133,985,469 GPC3, RPSAP63, 2 more genes
    nsv5200295copy number variation1nstd102humanPathogenic GRCh37 chrX: 132,717,085-132,924,462 , GRCh38.p12 chrX: 133,583,057-133,790,435 RPS24P19, RPSAP63, 1 more genes
    nsv997173copy number variation1nstd45humanPathogenic GRCh37 chrX: 132,669,773-133,119,673 , GRCh38.p12 chrX: 133,535,745-133,985,646 GPC3, RPS24P19, 2 more genes
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