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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv997106copy number variation1nstd45humanPathogenic NCBI36 (hg18) chrX: 21,960,842-22,176,399 , GRCh37 (hg19) chrX: 22,050,921-22,266,478 , GRCh38 (hg38) chrX: 22,032,803-22,248,361 PTCHD1-AS, PHEX-AS1, 1 more genes
    nsv3110107copy number variation1nstd37humanPathogenic NCBI36 (hg18) chrX: 1-54,147,138 , GRCh37 (hg19) chrX: 60,001-53,957,191 , GRCh38 (hg38) chrX: 10,001-54,103,980 GAGE12F, GS1-600G8.3, 400 more genes
    nsv3110105copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 168,547-112,474,026 , GRCh38 (hg38) chrX: 251,880-113,230,799 , NCBI36 (hg18) chrX: 108,547-112,360,682 GAGE12F, GS1-600G8.3, 711 more genes
    nsv3110097copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chrX: 21,708,594-22,054,641 , GRCh38 (hg38) chrX: 21,690,476-22,036,523 , NCBI36 (hg18) chrX: 21,618,515-21,964,562 SMPX, YY2, 3 more genes
    nsv3109777copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 168,546-35,841,052 , GRCh38 (hg38) chrX: 251,879-35,822,935 , NCBI36 (hg18) chrX: 108,546-35,750,973 GS1-600G8.3, LINC01546, 192 more genes
    esv4010954copy number variation1estd233human GRCh37 (hg19) chrX: 20,406,000-23,440,000 , GRCh38 (hg38) chrX: 20,387,882-23,421,883 PTCHD1-AS, PHEX-AS1, 11 more genes
    nsv3108927mobile element insertion1nstd144human GRCh37 (hg19) chrX: 22,172,226-22,172,226 , GRCh38 (hg38) chrX: 22,154,109-22,154,109 PHEX
    nsv3099496mobile element insertion1nstd144human GRCh37 (hg19) chrX: 22,243,110-22,243,110 , GRCh38 (hg38) chrX: 22,224,993-22,224,993 PTCHD1-AS, PHEX
    nsv3059880insertion1nstd140human GRCh37 (hg19) chrX: 22,243,092-22,243,093 , GRCh38 (hg38) chrX: 22,224,975-22,224,976 PTCHD1-AS, PHEX
    nsv3051842insertion1nstd140human GRCh38 (hg38) chrX: 22,224,994-22,224,995 , GRCh37 (hg19) chrX: 22,243,111-22,243,112 PTCHD1-AS, PHEX
    nsv2820428insertion1nstd137human GRCh38 (hg38) chrX: 22,224,957-22,224,957 , GRCh37 (hg19) chrX: 22,243,074-22,243,074 PTCHD1-AS, PHEX
    nsv2778891copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 168,546-155,196,888 , GRCh38 (hg38) chrX: 251,879-155,967,223 , NCBI36 (hg18) chrX: 108,546-154,850,082 GAGE12F, ZBTB33, 1116 more genes
    nsv2778309copy number variation2nstd37humanPathogenic GRCh37 (hg19) chrX: 22,166,967-22,219,901 , GRCh38 (hg38) chrX: 22,148,850-22,201,784 , NCBI36 (hg18) chrX: 22,076,888-22,129,822 PTCHD1-AS, PHEX-AS1, 1 more genes
    nsv2778279copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chrX: 350,431-154,913,754 , GRCh37 (hg19) chrX: 430,431-155,260,560 , GRCh38 (hg38) chrX: 469,696-156,030,895 GAGE12F, ZBTB33, 1114 more genes
    nsv2778274copy number variation3nstd37humanBenign GRCh37 (hg19) chrX: 22,129,362-22,129,540 , GRCh38 (hg38) chrX: 22,111,244-22,111,422 , NCBI36 (hg18) chrX: 22,039,283-22,039,461 PHEX
    nsv2778131copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 168,546-58,527,164 , GRCh38 (hg38) chrX: 251,879-58,500,731 , NCBI36 (hg18) chrX: 108,546-58,543,889 GAGE12F, GS1-600G8.3, 434 more genes
    nsv2777599copy number variation1nstd37humanPathogenic NCBI36 (hg18) chrX: 701-154,880,085 , GRCh37 (hg19) chrX: 60,701-155,226,891 , GRCh38 (hg38) chrX: 10,701-155,997,226 GAGE12F, ZBTB33, 1116 more genes
    nsv2777548copy number variation1nstd37humanPathogenic NCBI36 (hg18) chrX: 6,463,129-154,913,754 , GRCh37 (hg19) chrX: 6,453,129-155,260,560 , GRCh38 (hg38) chrX: 6,535,088-156,030,895 GAGE12F, ZBTB33, 1079 more genes
    nsv2777373copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 176,426-155,255,792 , GRCh38 (hg38) chrX: 259,759-156,026,127 , NCBI36 (hg18) chrX: 116,426-154,908,986 GAGE12F, ZBTB33, 1118 more genes
    nsv2777337copy number variation1nstd37humanPathogenic NCBI36 (hg18) chrX: 701-154,862,218 , GRCh37 (hg19) chrX: 60,701-155,209,024 , GRCh38 (hg38) chrX: 10,701-155,979,359 GAGE12F, ZBTB33, 1116 more genes
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