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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.p13 chrX: 137,887,441-155,232,907 , GRCh38.p12 chrX: 138,805,279-156,003,242 TREX2, LOC105373381, 327 more genes
    nsv3109988copy number variation1nstd37humanPathogenic NCBI36 (hg18) chrX: 72,986,649-154,881,025 , GRCh37.p13 chrX: 73,069,924-155,227,831 , GRCh38.p12 chrX: 73,850,089-155,998,166 TREX2, LOC100131072, 1165 more genes
    nsv3109874copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 151,201,777-154,741,703 , GRCh38.p12 chrX: 152,033,305-155,512,042 , NCBI36 (hg18) chrX: 150,952,433-154,394,897 TREX2, ABCD1, 154 more genes
    nsv3109872copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 146,232,592-155,233,731 , GRCh38.p12 chrX: 147,151,074-156,004,066 , NCBI36 (hg18) chrX: 146,040,284-154,886,925 TREX2, PRRG3, 245 more genes
    nsv3109772copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 112,474,054-155,233,731 , GRCh38.p12 chrX: 113,230,827-156,004,066 , NCBI36 (hg18) chrX: 112,360,710-154,886,925 TREX2, FATE1, 717 more genes
    nsv2786917copy number variation1nstd132human NCBI36 (hg18) chrX: 152,323,546-152,408,463 , GRCh37.p13 chrX|NW_003871103.3: 838,877-923,794 , GRCh37.p13 chrX: 152,670,352-152,755,269 , GRCh38.p12 chrX: 153,404,894-153,489,811 TREX2, PNMA6E, 5 more genes
    nsv2782073copy number variation1nstd132human NCBI36 (hg18) chrX: 152,323,546-152,968,184 , GRCh37.p13 chrX|NW_003871103.3: 838,877-1,483,518 , GRCh37.p13 chrX: 152,670,352-153,314,990 , GRCh38.p12 chrX: 153,404,894-154,049,539 TREX2, ABCD1, 39 more genes
    nsv2779113copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 31,088,082-155,233,731 , GRCh38.p12 chrX: 31,069,965-156,004,066 , NCBI36 (hg18) chrX: 30,998,003-154,886,925 TREX2, RNU6-49P, 1843 more genes
    nsv2779003copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chrX: 152,559,822-153,104,847 , GRCh38.p12 chrX: 153,294,364-153,839,392 , NCBI36 (hg18) chrX: 152,213,016-152,758,041 TREX2, LOC105373381, 29 more genes
    nsv2778891copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 168,546-155,196,888 , GRCh38.p12 chrX: 251,879-155,967,223 , NCBI36 (hg18) chrX: 108,546-154,850,082 TREX2, SLC25A6, 2182 more genes
    nsv2778279copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chrX: 350,431-154,913,754 , GRCh37.p13 chrX: 430,431-155,260,560 , GRCh38.p12 chrX: 469,696-156,030,895 TREX2, ABCB7, 2184 more genes
    nsv2777599copy number variation1nstd37humanPathogenic NCBI36 (hg18) chrX: 701-154,880,085 , GRCh37.p13 chrX: 60,701-155,226,891 , GRCh38.p12 chrX: 10,701-155,997,226 TREX2, ARR3, 2185 more genes
    nsv2777548copy number variation1nstd37humanPathogenic NCBI36 (hg18) chrX: 6,463,129-154,913,754 , GRCh37.p13 chrX: 6,453,129-155,260,560 , GRCh38.p12 chrX: 6,535,088-156,030,895 TREX2, ARR3, 2112 more genes
    nsv2777373copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 176,426-155,255,792 , GRCh38.p12 chrX: 259,759-156,026,127 , NCBI36 (hg18) chrX: 116,426-154,908,986 TREX2, NR0B1, 2188 more genes
    nsv2777337copy number variation1nstd37humanPathogenic NCBI36 (hg18) chrX: 701-154,862,218 , GRCh37.p13 chrX: 60,701-155,209,024 , GRCh38.p12 chrX: 10,701-155,979,359 TREX2, SLC25A6, 2183 more genes
    nsv2777238copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chrX: 1,498,662-154,913,754 , GRCh37.p13 chrX: 1,538,662-155,260,560 , GRCh38.p12 chrX: 1,419,769-156,030,895 TREX2, NR0B1, 2164 more genes
    nsv2776801copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 94,043,221-155,246,585 , GRCh38.p12 chrX: 94,788,222-156,016,920 , NCBI36 (hg18) chrX: 93,929,877-154,899,779 TREX2, ARHGAP4, 975 more genes
    nsv2776723copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chrX: 228,188-154,913,754 , GRCh37.p13 chrX: 308,188-155,260,560 , GRCh38.p12 chrX: 347,453-156,030,895 TREX2, NR0B1, 2185 more genes
    nsv2776439copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 56,457,791-155,233,731 , GRCh38.p12 chrX: 56,431,358-156,004,066 , NCBI36 (hg18) chrX: 56,474,516-154,886,925 TREX2, LOC728317, 1376 more genes
    nsv2776244copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 133,944,147-155,233,731 , GRCh38.p12 chrX: 134,810,117-156,004,066 , NCBI36 (hg18) chrX: 133,771,813-154,886,925 TREX2, NCLP2, 414 more genes
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