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Results: 1 to 20 of 220

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Number of Variants: 20

Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
nsv1067634copy number variation8nstd101humanPathogenic GRCh37 (hg19) chrX: 76,102-155,226,096 , GRCh38 (hg38) chrX: 26,102-155,996,431 , NCBI36 (hg18) chrX: 16,102-154,879,290 GAGE12F, ZBTB33, 1060 more genes
nsv1067633copy number variation2nstd101humanPathogenic GRCh37 (hg19) chrX: 64,245-155,228,958 , GRCh38 (hg38) chrX: 14,245-155,999,293 , NCBI36 (hg18) chrX: 4,245-154,882,152 GAGE12F, ZBTB33, 1061 more genes
nsv1067632copy number variation16nstd101humanPathogenic GRCh37 (hg19) chrX: 60,679-155,251,871 , GRCh38 (hg38) chrX: 10,679-156,022,206 , NCBI36 (hg18) chrX: 679-154,905,065 GAGE12F, ZBTB33, 1061 more genes
nsv1067631copy number variation3nstd101humanPathogenic GRCh37 (hg19) chrX: 60,679-155,242,832 , GRCh38 (hg38) chrX: 10,679-156,013,167 , NCBI36 (hg18) chrX: 679-154,896,026 GAGE12F, ZBTB33, 1061 more genes
nsv997094copy number variation1nstd45humanPathogenic GRCh37 (hg19) chrX: 14,861,529-14,891,184 , GRCh38 (hg38) chrX: 14,843,407-14,873,062 , NCBI36 (hg18) chrX: 14,771,450-14,801,105 FANCB
nsv996272copy number variation1nstd37humanLikely pathogenic GRCh37 (hg19) chrX: 12,874,859-19,398,435 , GRCh38 (hg38) chrX: 12,856,740-19,380,317 , NCBI36 (hg18) chrX: 12,784,780-19,308,356 GS1-600G8.3, PHKA2-AS1, 55 more genes
nsv996242copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 168,547-65,665,687 , GRCh38 (hg38) chrX: 251,880-66,445,845 , NCBI36 (hg18) chrX: 108,547-65,582,412 GAGE12F, GS1-600G8.3, 424 more genes
nsv995933copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 168,546-117,981,120 , GRCh38 (hg38) chrX: 251,879-118,847,157 , NCBI36 (hg18) chrX: 108,546-117,865,148 GAGE12F, GS1-600G8.3, 704 more genes
nsv995783copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 168,546-16,985,413 , GRCh38 (hg38) chrX: 251,879-16,967,290 , NCBI36 (hg18) chrX: 108,546-16,895,334 GS1-600G8.3, LINC01546, 101 more genes
nsv995748copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 168,547-51,386,559 , GRCh38 (hg38) chrX: 251,880-51,643,625 , NCBI36 (hg18) chrX: 108,547-51,403,299 GAGE12F, GS1-600G8.3, 339 more genes
nsv995520copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 168,546-35,903,121 , GRCh38 (hg38) chrX: 251,879-35,885,004 , NCBI36 (hg18) chrX: 108,546-35,813,042 GS1-600G8.3, LINC01546, 180 more genes
nsv995406copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 168,546-16,275,578 , GRCh38 (hg38) chrX: 251,879-16,257,455 , NCBI36 (hg18) chrX: 108,546-16,185,499 GS1-600G8.3, LINC01546, 94 more genes
nsv995375copy number variation11nstd37humanPathogenic GRCh37 (hg19) chrX: 168,546-155,233,731 , GRCh38 (hg38) chrX: 251,879-156,004,066 , NCBI36 (hg18) chrX: 108,546-154,886,925 GAGE12F, ZBTB33, 1061 more genes
nsv995296copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 168,546-50,032,363 , GRCh38 (hg38) chrX: 251,879-50,289,363 , NCBI36 (hg18) chrX: 108,546-50,049,103 GAGE12F, GS1-600G8.3, 329 more genes
nsv993511copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 70,297-155,246,585 , GRCh38 (hg38) chrX: 20,297-156,016,920 , NCBI36 (hg18) chrX: 10,297-154,899,779 GAGE12F, ZBTB33, 1061 more genes
nsv993510copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 2,217,264-155,221,853 , GRCh38 (hg38) chrX: 2,299,223-155,992,188 , NCBI36 (hg18) chrX: 2,227,264-154,875,047 GAGE12F, ZBTB33, 1045 more genes
nsv993499copy number variation1nstd37humanPathogenic NCBI36 (hg18) chrX: 701-53,177,098 , GRCh37 (hg19) chrX: 60,701-53,160,373 , GRCh38 (hg38) chrX: 10,701-53,131,191 GAGE12F, GS1-600G8.3, 365 more genes
nsv984830copy number variation2nstd11humannot provided NCBI36 (hg18) chrX: 108,477-154,887,040 , GRCh37 (hg19) chrX: 168,477-155,233,846 , GRCh38 (hg38) chrX: 251,810-156,004,181 GAGE12F, ZBTB33, 1061 more genes
esv3421232copy number variation1estd59human NCBI36 (hg18) chrX: 14,800,602-14,802,600 , GRCh37 (hg19) chrX: 14,890,681-14,892,679 , GRCh38 (hg38) chrX: 14,872,559-14,874,557 MOSPD2, FANCB
esv2982735insertion1estd209human GRCh37 (hg19) chrX: 14,869,620-14,869,620 , GRCh38 (hg38) chrX: 14,851,498-14,851,498 FANCB

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