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Items: 1 to 20 of 264

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6313471copy number variation1nstd102humanPathogenic GRCh37 chrX: 8,501,036-8,591,731 , GRCh38.p12 chrX: 8,532,995-8,623,690 ANOS1
    nsv6315226copy number variation1nstd102humanPathogenic GRCh38 chrX: 8,531,912-8,535,179 , GRCh37 chrX: 8,499,953-8,503,220 ANOS1
    nsv997104copy number variation1nstd45humanPathogenic GRCh37 chrX: 8,496,915-8,700,228 , GRCh38.p12 chrX: 8,528,874-8,732,187 ANOS1
    nsv7098552copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chrX: 8,501,036-8,700,077 , GRCh38.p12 chrX: 8,532,995-8,732,036 ANOS1
    nsv4681395copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 8,521,973-8,565,317 , GRCh38.p12 chrX: 8,553,932-8,597,276 ANOS1
    nsv3905091copy number variation1nstd102humanLikely benign GRCh38 chrX: 8,629,706-8,736,954 , NCBI36 chrX: 8,557,747-8,664,995 , GRCh37 chrX: 8,597,747-8,704,995 ANOS1
    nsv3870944copy number variation2nstd102humanLikely benign GRCh37 chrX: 8,601,505-8,702,970 , GRCh38.p12 chrX: 8,633,464-8,734,929 ANOS1
    nsv3878561copy number variation1nstd102humanBenign GRCh37 chrX: 8,595,820-8,694,839 , GRCh38.p12 chrX: 8,627,779-8,726,798 ANOS1
    nsv3883988copy number variation1nstd102humanBenign GRCh37 chrX: 8,595,820-8,676,423 , GRCh38.p12 chrX: 8,627,779-8,708,382 ANOS1
    nsv4452979copy number variation1nstd102humanUncertain significance GRCh37 chrX: 8,588,404-8,603,599 , GRCh38.p12 chrX: 8,620,363-8,635,558 ANOS1
    nsv3890469copy number variation1nstd102humanUncertain significance GRCh37 chrX: 8,516,447-8,720,758 , GRCh38 chrX: 8,548,406-8,752,717 , NCBI36 chrX: 8,476,447-8,680,758 ANOS1
    nsv3906266copy number variation1nstd102humanUncertain significance NCBI36 chrX: 8,516,249-8,680,758 , GRCh38 chrX: 8,588,208-8,752,717 , GRCh37 chrX: 8,556,249-8,720,758 ANOS1
    nsv4450766copy number variation1nstd102humanUncertain significance GRCh38 chrX: 8,587,774-8,732,056 , GRCh37 chrX: 8,555,815-8,700,097 ANOS1
    nsv3918444copy number variation1nstd102humanUncertain significance NCBI36 chrX: 8,553,682-8,680,547 , GRCh37.p13 chrX: 8,593,682-8,720,547 , GRCh38.p12 chrX: 8,625,641-8,752,506 ANOS1
    nsv4451180copy number variation1nstd102humanUncertain significance GRCh37 chrX: 8,588,404-8,710,465 , GRCh38.p12 chrX: 8,620,363-8,742,424 ANOS1
    nsv3906743copy number variation1nstd102humanUncertain significance GRCh38 chrX: 8,619,710-8,740,650 , NCBI36 chrX: 8,547,751-8,668,691 , GRCh37 chrX: 8,587,751-8,708,691 ANOS1
    nsv3877599copy number variation1nstd102humanUncertain significance GRCh37 chrX: 8,588,402-8,702,277 , GRCh38.p12 chrX: 8,620,361-8,734,236 ANOS1
    nsv3897775copy number variation1nstd102humanUncertain significance NCBI36 chrX: 8,553,486-8,665,494 , GRCh37 chrX: 8,593,486-8,705,494 , GRCh38 chrX: 8,625,445-8,737,453 ANOS1
    nsv3900752copy number variation2nstd102humanUncertain significance GRCh37 chrX: 8,595,045-8,704,378 , GRCh38 chrX: 8,627,004-8,736,337 , NCBI36 chrX: 8,555,045-8,664,378 ANOS1
    nsv3907978copy number variation1nstd102humanUncertain significance GRCh38 chrX: 8,628,853-8,737,453 , GRCh37 chrX: 8,596,894-8,705,494 , NCBI36 chrX: 8,556,894-8,665,494 ANOS1
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