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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3157584copy number variation1nstd151human GRCh37 (hg19) chr9: 96,054,588-96,864,038 , GRCh38 (hg38) chr9: 93,292,306-94,101,756 BARX1, MIR4291, 14 more genes
    nsv3155222copy number variation1nstd151human GRCh37 (hg19) chr9: 96,062,331-96,860,957 , GRCh38 (hg38) chr9: 93,300,049-94,098,675 BARX1, FAM120AOS, 14 more genes
    nsv3144539copy number variation1nstd151human GRCh37 (hg19) chr9: 96,061,350-97,221,699 , GRCh38 (hg38) chr9: 93,299,068-94,459,417 BARX1, FAM120A, 29 more genes
    nsv3138543copy number variation1nstd151human GRCh37 (hg19) chr9: 96,714,443-99,327,797 , GRCh38 (hg38) chr9: 93,952,161-96,565,515 BARX1, FANCC, 68 more genes
    nsv2774488copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr9: 2,934-140,273,252 , GRCh37 (hg19) chr9: 12,934-141,153,431 , GRCh38 (hg38) chr9: 12,934-138,262,981 BARX1, ABCA2, 2268 more genes
    nsv2773152copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr9: 203,864-141,020,389 , GRCh38 (hg38) chr9: 203,864-138,125,937 , NCBI36 (hg18) chr9: 193,864-140,140,210 BARX1, ABL1, 2250 more genes
    nsv2756841copy number variation1nstd130human GRCh37 (hg19) chr9: 502,292-140,777,105 , GRCh38 (hg38) chr9: 502,292-137,882,653 BARX1, ABCA2, 2242 more genes
    nsv2745220copy number variation1nstd130human NCBI36 (hg18) chr9: 70,151,170-139,876,646 , GRCh37 (hg19) chr9: 71,130,848-140,756,825 , GRCh38 (hg38) chr9: 68,346,434-137,862,373 BARX1, ALAD, 1359 more genes
    nsv2735676copy number variation1nstd130human NCBI36 (hg18) chr9: 326,186-137,969,530 , GRCh37 (hg19) chr9: 336,186-138,829,709 , GRCh38 (hg38) chr9: 193,412-135,937,863 BARX1, ABL1, 2134 more genes
    nsv2735670copy number variation1nstd130human NCBI36 (hg18) chr9: 198,549-138,844,941 , GRCh37 (hg19) chr9: 208,549-139,725,120 , GRCh38 (hg38) chr9: 193,412-136,830,668 BARX1, ABCA1, 2183 more genes
    nsv2635021short tandem repeat2nstd128human GRCh37 (hg19) chr9: 96,713,850-96,713,876 , GRCh38 (hg38) chr9: 93,951,568-93,951,594 BARX1
    nsv2633949short tandem repeat2nstd128human GRCh37 (hg19) chr9: 96,712,906-96,712,922 , GRCh38 (hg38) chr9: 93,950,624-93,950,640 BARX1
    nsv2633724short tandem repeat1nstd128human GRCh37 (hg19) chr9: 96,720,649-96,720,663 , GRCh38 (hg38) chr9: 93,958,367-93,958,381 BARX1-DT
    nsv2633723short tandem repeat1nstd128human GRCh37 (hg19) chr9: 96,717,458-96,717,478 , GRCh38 (hg38) chr9: 93,955,176-93,955,196 BARX1, BARX1-DT
    nsv2633522short tandem repeat2nstd128human GRCh37 (hg19) chr9: 96,712,935-96,712,962 , GRCh38 (hg38) chr9: 93,950,653-93,950,680 BARX1
    nsv1358530copy number variation1nstd122human NCBI36 (hg18) chr9: 95,719,993-95,786,931 , GRCh37 (hg19) chr9: 96,680,172-96,747,110 , GRCh38 (hg38) chr9: 93,917,890-93,984,828 BARX1, BARX1-DT
    nsv1353882copy number variation1nstd122human NCBI36 (hg18) chr9: 95,748,843-95,768,950 , GRCh37 (hg19) chr9: 96,709,022-96,729,129 , GRCh38 (hg38) chr9: 93,946,740-93,966,847 BARX1, BARX1-DT
    nsv1188789copy number variation1nstd113human NCBI36 (hg18) chr9: 93,147,956-95,975,663 , GRCh37 (hg19) chr9: 94,108,135-96,935,842 , GRCh38 (hg38) chr9: 91,345,853-94,173,560 BARX1, ECM2, 72 more genes
    nsv1120065inversion1nstd106human GRCh37 (hg19) chr9: 33,504,892-100,012,786 , GRCh38 (hg38) chr9: 33,504,894-97,250,504 BARX1, NUDT2, 975 more genes
    nsv1113011copy number variation1nstd106human GRCh37 (hg19) chr9: 96,717,300-96,717,800 , GRCh38 (hg38) chr9: 93,955,018-93,955,518 BARX1, BARX1-DT
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