Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 466

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv2820503insertion1nstd137human GRCh38 (hg38) chrX: 45,040,327-45,040,327 , GRCh37 (hg19) chrX: 44,899,572-44,899,572 KDM6A
    nsv2781863complex chromosomal rearrangement2nstd133human GRCh37 (hg19) chr5: 176,906,708-176,906,708 , GRCh37 (hg19) chr5: 176,906,713-176,906,713 , GRCh37 (hg19) chrX: 44,759,733-44,759,733 , GRCh37 (hg19) chrX: 44,759,735-44,759,735 , GRCh38 (hg38) chr5: 177,479,707-177,479,707 , GRCh38 (hg38) chr5: 177,479,712-177,479,712 , GRCh38 (hg38) chrX: 44,900,487-44,900,487 , GRCh38 (hg38) chrX: 44,900,489-44,900,489 DBN1, KDM6A
    nsv2781812complex chromosomal rearrangement2nstd133human GRCh37 (hg19) chrX: 44,893,800-44,893,800 , GRCh37 (hg19) chrX: 44,901,361-44,901,361 , GRCh37 (hg19) chrX: 117,134,725-117,134,725 , GRCh37 (hg19) chrX: 117,140,815-117,140,815 , GRCh38 (hg38) chrX: 118,006,852-118,006,852 , GRCh38 (hg38) chrX: 45,034,555-45,034,555 , GRCh38 (hg38) chrX: 45,042,116-45,042,116 , GRCh38 (hg38) chrX: 118,000,762-118,000,762 KDM6A, KLHL13
    nsv2779113copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 31,088,082-155,233,731 , GRCh38 (hg38) chrX: 31,069,965-156,004,066 , NCBI36 (hg18) chrX: 30,998,003-154,886,925 GAGE12F, ZBTB33, 931 more genes
    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, 1112 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, 1110 more genes
    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, 431 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, 1112 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, 1077 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, 1114 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, 1112 more genes
    nsv2777238copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chrX: 1,498,662-154,913,754 , GRCh37 (hg19) chrX: 1,538,662-155,260,560 , GRCh38 (hg38) chrX: 1,419,769-156,030,895 GAGE12F, ZBTB33, 1102 more genes
    nsv2777109copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chrX: 44,815,967-45,034,034 , GRCh38 (hg38) chrX: 44,956,722-45,174,789 , NCBI36 (hg18) chrX: 44,700,911-44,918,978 KDM6A, CXorf36
    nsv2776723copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chrX: 228,188-154,913,754 , GRCh37 (hg19) chrX: 308,188-155,260,560 , GRCh38 (hg38) chrX: 347,453-156,030,895 GAGE12F, ZBTB33, 1111 more genes
    nsv2776482copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 168,546-54,996,659 , GRCh38 (hg38) chrX: 251,879-54,970,226 , NCBI36 (hg18) chrX: 108,546-55,013,384 GAGE12F, GS1-600G8.3, 406 more genes
    nsv2775834copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 553,069-155,233,731 , GRCh38 (hg38) chrX: 592,334-156,004,066 , NCBI36 (hg18) chrX: 473,069-154,886,925 GAGE12F, ZBTB33, 1109 more genes
    nsv2775505copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 37,521,774-98,488,534 , GRCh38 (hg38) chrX: 37,662,521-99,233,536 , NCBI36 (hg18) chrX: 37,406,693-98,375,190 GAGE12F, SNORA11C, 388 more genes
    nsv2775492copy number variation1nstd37humanLikely pathogenic GRCh37 (hg19) chrX: 40,933,552-45,379,179 , GRCh38 (hg38) chrX: 41,074,299-45,519,934 , NCBI36 (hg18) chrX: 40,818,496-45,264,123 RNA5SP502, LINC01204, 14 more genes
    nsv2774840copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 168,546-155,081,533 , GRCh38 (hg38) chrX: 251,879-155,851,870 , NCBI36 (hg18) chrX: 108,546-154,734,727 GAGE12F, ZBTB33, 1111 more genes
    nsv2774799copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 168,547-151,304,063 , GRCh38 (hg38) chrX: 251,880-152,135,591 , NCBI36 (hg18) chrX: 108,547-151,054,719 GAGE12F, ZBTB33, 999 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Find related data

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    Support Center