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Items: 1 to 20 of 209

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096312copy number variation1nstd102humanUncertain significance GRCh37 chr22: 40,741,451-40,859,231 , GRCh38.p12 chr22: 40,345,447-40,463,227 SGSM3-AS1, ADSL, 2 more genes
    nsv7096308copy number variation1nstd102humanUncertain significance GRCh37 chr22: 35,776,672-42,486,826 , GRCh38.p12 chr22: 35,380,679-42,090,822 CDC42EP1, SREBF2, 231 more genes
    nsv7077764inversion1nstd229human GRCh38 chr22: 37,971,370-41,589,449 , GRCh37.p13 chr22: 38,367,377-41,985,453 UQCRFS1P1, LOC105373027, 119 more genes
    nsv7064338inversion1nstd229human GRCh38 chr22: 40,322,864-40,533,291 , GRCh37.p13 chr22: 40,718,868-40,929,295 ADSL, SGSM3, 4 more genes
    nsv7061959inversion1nstd229human GRCh38 chr22: 36,818,005-44,993,640 , GRCh37.p13 chr22: 37,214,049-45,389,520 SMIM45, A4GALT, 271 more genes
    nsv7058666inversion1nstd229human GRCh38 chr22: 39,066,437-42,707,681 , GRCh37.p13 chr22: 39,462,442-43,103,687 LOC101927344, ATF4, 128 more genes
    nsv7036676copy number variation1nstd229human GRCh38 chr22: 40,405,313-40,405,370 , GRCh37.p13 chr22: 40,801,317-40,801,374 SGSM3
    nsv7033455copy number variation1nstd229human GRCh38 chr22: 40,375,228-40,386,332 , GRCh37.p13 chr22: 40,771,232-40,782,336 SGSM3-AS1, ADSL, 1 more genes
    nsv7031634copy number variation1nstd229human GRCh38 chr22: 40,410,282-40,410,408 , GRCh37.p13 chr22: 40,806,286-40,806,412 SGSM3, MRTFA
    nsv7028690copy number variation1nstd229human GRCh38 chr22: 40,347,668-40,374,816 , GRCh37.p13 chr22: 40,743,672-40,770,820 ADSL, SGSM3-AS1, 1 more genes
    nsv7027764copy number variation1nstd229human GRCh38 chr22: 40,390,843-40,393,708 , GRCh37.p13 chr22: 40,786,847-40,789,712 SGSM3
    nsv7027741copy number variation1nstd229human GRCh38 chr22: 39,432,386-49,047,389 , GRCh37.p13 chr22: 39,828,391-49,443,201 LOC105373064, ACO2, 233 more genes
    nsv7019974copy number variation1nstd229human GRCh38 chr22: 40,380,060-40,386,372 , GRCh37.p13 chr22: 40,776,064-40,782,376 SGSM3, ADSL, 1 more genes
    nsv7019774copy number variation1nstd229human GRCh38 chr22: 40,378,679-40,384,735 , GRCh37.p13 chr22: 40,774,683-40,780,739 ADSL, SGSM3, 1 more genes
    nsv7019741copy number variation1nstd229human GRCh38 chr22: 40,374,419-40,383,330 , GRCh37.p13 chr22: 40,770,423-40,779,334 SGSM3-AS1, SGSM3, 1 more genes
    nsv6638050copy number variation1nstd102humanPathogenic GRCh37 chr22: 40,131,240-41,556,564 , GRCh38.p12 chr22: 39,735,235-41,160,560 GRAP2, UQCRFS1P1, 32 more genes
    nsv6637214copy number variation1nstd102humanUncertain significance GRCh37 chr22: 39,768,795-41,946,225 , GRCh38.p12 chr22: 39,372,790-41,550,221 MRTFA-AS1, LOC105373043, 62 more genes
    nsv6635717copy number variation1nstd227human GRCh38.p12 chr22: 40,369,106-40,407,182 , GRCh37 chr22: 40,765,110-40,803,186 ADSL, SGSM3, 1 more genes
    nsv6627461copy number variation1nstd224human GRCh37 chr22: 40,742,567-40,862,120 , GRCh38.p12 chr22: 40,346,563-40,466,116 MRTFA, ADSL, 2 more genes
    nsv6598643inversion1nstd223human GRCh38 chr22: 40,394,636-40,395,326 , GRCh37.p13 chr22: 40,790,640-40,791,330 SGSM3
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