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Items: 1 to 20 of 295

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5874629copy number variation1nstd209human GRCh38 chrX: 92,112,536-92,113,795 , GRCh37.p13 chrX: 91,367,535-91,368,794 EIF4A1P10, PCDH11X
    nsv5667020copy number variation1nstd207human GRCh38 chrX: 92,112,536-92,113,795 , GRCh37.p13 chrX: 91,367,535-91,368,794 PCDH11X, EIF4A1P10
    nsv5383109copy number variation1nstd186human GRCh37 chrX: 91,367,528-91,368,794 , GRCh38.p12 chrX: 92,112,529-92,113,795 PCDH11X, EIF4A1P10
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4905752copy number variation1nstd200human GRCh38 chrX: 92,014,668-92,640,702 , GRCh37.p13 chrX: 91,269,667-91,895,701 EIF4A1P10, PCDH11X, 2 more genes
    nsv4771848copy number variation1nstd200human GRCh37 chrX: 91,367,527-91,368,795 , GRCh38.p12 chrX: 92,112,528-92,113,796 PCDH11X, EIF4A1P10
    nsv4771847copy number variation1nstd200human GRCh37 chrX: 91,361,191-91,464,497 , GRCh38.p12 chrX: 92,106,192-92,209,498 PCDH11X, EIF4A1P10
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
    nsv4728601copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,514,079-127,770,854 , GRCh38.p12 chrX: 78,258,582-128,636,876 PHB1P10, SNORA35, 565 more genes
    nsv4728499copy number variation1nstd102humanPathogenic GRCh37 chrX: 55,507,789-155,198,481 , GRCh38.p12 chrX: 55,481,356-155,968,816 GABRE, RN7SL325P, 1371 more genes
    nsv4674753copy number variation1nstd102humanPathogenic GRCh37 chrX: 78,444,738-155,233,731 , GRCh38.p12 chrX: 79,189,241-156,004,066 PAK3, ZCCHC12, 1069 more genes
    nsv4674080copy number variation1nstd102humanPathogenic GRCh37 chrX: 84,387,417-155,233,731 , GRCh38.p12 chrX: 85,132,411-156,004,066 CSTF2, GPR119, 1029 more genes
    nsv4661940copy number variation1nstd186human GRCh37 chrX: 91,367,535-91,368,795 , GRCh38.p12 chrX: 92,112,536-92,113,796 EIF4A1P10, PCDH11X
    nsv4645669copy number variation1nstd186human GRCh37 chrX: 91,367,532-91,368,793 , GRCh38.p12 chrX: 92,112,533-92,113,794 PCDH11X, EIF4A1P10
    nsv4641167copy number variation1nstd186human GRCh37 chrX: 91,367,538-91,368,795 , GRCh38.p12 chrX: 92,112,539-92,113,796 EIF4A1P10, PCDH11X
    nsv4630842copy number variation1nstd183human GRCh37 chrX: 90,750,580-91,427,682 , GRCh38.p12 chrX: 91,495,581-92,172,683 PCDH11X, SERBP1P4, 4 more genes
    nsv4627533copy number variation1nstd183human GRCh37 chrX: 91,367,535-91,368,795 , GRCh38.p12 chrX: 92,112,536-92,113,796 EIF4A1P10, PCDH11X
    nsv4517002copy number variation1nstd166human GRCh37.p13 chrX: 90,680,999-91,405,650 , GRCh38.p12 chrX: 91,426,000-92,150,651 PCDH11X, PABPC5, 6 more genes
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