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Results: 1 to 20 of 146

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Number of Variants: 20

Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
esv3631719mobile element insertion210estd214human GRCh37 (hg19) chr13: 32,922,439-32,922,439 , GRCh38 (hg38) chr13: 32,348,302-32,348,302 BRCA2
nsv1067714copy number variation2nstd101humanPathogenic NCBI36 (hg18) chr13: 19,309,535-114,110,750 , GRCh37 (hg19) chr13: 20,411,535-115,085,141 , GRCh38 (hg38) chr13: 19,837,395-114,327,173 POLR2KP2, LINC00462, 540 more genes
nsv1067712copy number variation1nstd101humanPathogenic NCBI36 (hg18) chr13: 30,835,609-90,025,547 , GRCh37 (hg19) chr13: 31,937,609-91,227,546 , GRCh38 (hg38) chr13: 31,363,472-90,575,292 POLR2KP2, LINC00462, 274 more genes
esv3580597copy number variation1estd212human GRCh38 chr13: 32,133,371-32,386,655 , GRCh37 (hg19) chr13: 32,707,508-32,960,792 FRY, ZAR1L, 1 more genes
nsv1052467copy number variation1nstd100human NCBI36 (hg18) chr13: 29,645,540-45,095,836 , GRCh37 (hg19) chr13: 30,747,540-46,197,835 , GRCh38 (hg38) chr13: 30,173,403-45,623,700 LINC00426, TRE-TTC2-1, 115 more genes
nsv1051748copy number variation1nstd100human NCBI36 (hg18) chr13: 18,242,164-114,096,042 , GRCh37 (hg19) chr13: 19,344,164-115,077,940 , GRCh38 (hg38) chr13: 18,770,024-114,312,465 POLR2KP2, LINC00462, 550 more genes
nsv1048681copy number variation1nstd100human NCBI36 (hg18) chr13: 29,128,098-33,885,086 , GRCh37 (hg19) chr13: 30,230,098-34,987,086 , GRCh38 (hg38) chr13: 29,655,961-34,412,949 LINC00426, TRN-GTT2-4, 33 more genes
nsv1045499copy number variation1nstd100human NCBI36 (hg18) chr13: 18,242,164-114,096,043 , GRCh37 (hg19) chr13: 19,344,164-115,077,941 , GRCh38 (hg38) chr13: 18,770,024-114,312,466 POLR2KP2, LINC00462, 550 more genes
nsv1041605copy number variation4nstd100human NCBI36 (hg18) chr13: 18,454,945-114,109,838 , GRCh37 (hg19) chr13: 19,556,945-115,091,736 , GRCh38 (hg38) chr13: 18,982,805-114,326,261 POLR2KP2, LINC00462, 548 more genes
nsv1038898copy number variation1nstd100human NCBI36 (hg18) chr13: 18,361,437-114,096,183 , GRCh37 (hg19) chr13: 19,463,437-115,078,081 , GRCh38 (hg38) chr13: 18,889,297-114,312,606 POLR2KP2, LINC00462, 548 more genes
nsv997202copy number variation1nstd45humanPathogenic GRCh37 (hg19) chr13: 32,889,617-32,973,809 , GRCh38 (hg38) chr13: 32,315,480-32,399,672 , NCBI36 (hg18) chr13: 31,787,617-31,871,809 BRCA2
esv3567869copy number variation1estd211human GRCh37 (hg19) chr13: 32,256,242-38,753,675 , GRCh38 chr13: 31,682,105-38,179,538 FRY-AS1, LINC00445, 38 more genes
esv3550285copy number variation1estd215human GRCh37 (hg19) chr13: 32,960,704-32,960,735 , GRCh38 chr13: 32,386,567-32,386,598 BRCA2
nsv995497copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr13: 19,436,286-34,151,488 , GRCh38 (hg38) chr13: 18,862,146-33,577,351 , NCBI36 (hg18) chr13: 18,334,286-33,049,488 LINC00426, TRN-GTT2-4, 127 more genes
nsv995433copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr13: 19,436,286-115,107,733 , GRCh38 (hg38) chr13: 18,862,146-114,342,258 , NCBI36 (hg18) chr13: 18,334,286-114,125,835 POLR2KP2, LINC00462, 551 more genes
nsv989279mobile element insertion4nstd94human GRCh37 (hg19) chr13: 32,922,433-32,922,434 , GRCh38 chr13: 32,348,296-32,348,297 BRCA2
nsv984840copy number variation2nstd11humannot provided GRCh37 (hg19) chr13: 19,026,949-115,108,397 , NCBI36 (hg18) chr13: 17,924,949-114,126,499 , GRCh38 chr13: 18,452,809-114,342,922 POLR2KP2, LINC00462, 550 more genes
esv3426269insertion15estd59human NCBI36 (hg18) chr13: 31,820,415-31,820,457 , GRCh37 (hg19) chr13: 32,922,415-32,922,457 , GRCh38 chr13: 32,348,278-32,348,320 BRCA2
esv3416309copy number variation1estd59human NCBI36 (hg18) chr13: 31,837,728-32,232,364 , GRCh37 (hg19) chr13: 32,939,728-33,334,364 , GRCh38 chr13: 32,365,591-32,760,226 N4BP2L2, N4BP2L2-IT2, 3 more genes
esv3413358copy number variation1estd59human NCBI36 (hg18) chr13: 31,837,324-31,837,758 , GRCh37 (hg19) chr13: 32,939,324-32,939,758 , GRCh38 chr13: 32,365,187-32,365,621 BRCA2

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