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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3110092copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chrX: 137,715,107-154,886,101 , GRCh37 (hg19) chrX: 137,887,441-155,232,907 , GRCh38 (hg38) chrX: 138,805,279-156,003,242 SLC6A8, TWF1P2, 327 more genes
    nsv3109988copy number variation1nstd37humanPathogenic NCBI36 (hg18) chrX: 72,986,649-154,881,025 , GRCh37 (hg19) chrX: 73,069,924-155,227,831 , GRCh38 (hg38) chrX: 73,850,089-155,998,166 SLC6A8, RNU6-496P, 1165 more genes
    nsv3109874copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 151,201,777-154,741,703 , GRCh38 (hg38) chrX: 152,033,305-155,512,042 , NCBI36 (hg18) chrX: 150,952,433-154,394,897 SLC6A8, CETN2, 154 more genes
    nsv3109872copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 146,232,592-155,233,731 , GRCh38 (hg38) chrX: 147,151,074-156,004,066 , NCBI36 (hg18) chrX: 146,040,284-154,886,925 SLC6A8, HSFX4, 245 more genes
    nsv3109772copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 112,474,054-155,233,731 , GRCh38 (hg38) chrX: 113,230,827-156,004,066 , NCBI36 (hg18) chrX: 112,360,710-154,886,925 SLC6A8, CSAG4, 717 more genes
    nsv2782073copy number variation1nstd132human NCBI36 (hg18) chrX: 152,323,546-152,968,184 , GRCh37 (hg19) chrX: 152,670,352-153,314,990 , GRCh37.p13 chrX|NW_003871103.3: 838,877-1,483,518 , GRCh38 (hg38) chrX: 153,404,894-154,049,539 SLC6A8, ABCD1, 39 more genes
    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 SLC6A8, GLUD1P9, 1843 more genes
    nsv2779003copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chrX: 152,559,822-153,104,847 , GRCh38 (hg38) chrX: 153,294,364-153,839,392 , NCBI36 (hg18) chrX: 152,213,016-152,758,041 SLC6A8, ATP2B3, 29 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 SLC6A8, NR0B1, 2183 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 SLC6A8, ARR3, 2185 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 SLC6A8, AMELX, 2186 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 SLC6A8, ABCB7, 2113 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 SLC6A8, ABCB7, 2189 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 SLC6A8, NR0B1, 2184 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 SLC6A8, AMELX, 2165 more genes
    nsv2776801copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 94,043,221-155,246,585 , GRCh38 (hg38) chrX: 94,788,222-156,016,920 , NCBI36 (hg18) chrX: 93,929,877-154,899,779 SLC6A8, XIAP, 975 more genes
    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 SLC6A8, ABCB7, 2186 more genes
    nsv2776439copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 56,457,791-155,233,731 , GRCh38 (hg38) chrX: 56,431,358-156,004,066 , NCBI36 (hg18) chrX: 56,474,516-154,886,925 SLC6A8, ETDA, 1376 more genes
    nsv2776244copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 133,944,147-155,233,731 , GRCh38 (hg38) chrX: 134,810,117-156,004,066 , NCBI36 (hg18) chrX: 133,771,813-154,886,925 SLC6A8, RNA5SP524, 414 more genes
    nsv2776118copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 78,230,501-155,233,731 , GRCh38 (hg38) chrX: 78,975,004-156,004,066 , NCBI36 (hg18) chrX: 78,117,157-154,886,925 SLC6A8, SPANXN2, 1080 more genes
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