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Results: 1 to 20 of 25

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Number of Variants: 20

Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
nsv984837copy number variation2nstd11humannot provided GRCh37 (hg19) chr3: 60,345-197,896,118 , NCBI36 (hg18) chr3: 35,345-199,380,515 , GRCh38 chr3: 18,667-198,169,247 ZBTB11-AS1, SNORD19B, 1352 more genes
esv3369810copy number variation1estd59human NCBI36 (hg18) chr3: 92,774-75,780,040 , GRCh37 (hg19) chr3: 117,774-75,697,350 , GRCh38 chr3: 76,091-75,648,199 SNORD19B, MIR885, 604 more genes
esv3323803copy number variation1estd59human NCBI36 (hg18) chr3: 23,705,741-121,059,389 , GRCh37 (hg19) chr3: 23,730,737-119,576,699 , GRCh38 chr3: 23,689,246-119,857,852 ZBTB11-AS1, SNORD19B, 634 more genes
nsv949732copy number variation1nstd85human NCBI35 (hg17) chr3: 43,662,277-46,983,297 , GRCh37 (hg19) chr3: 43,687,273-47,008,293 , GRCh38 chr3: 43,645,781-46,966,803 TRNAR11, PRSS46, 51 more genes
esv2757869copy number variation30estd1human NCBI35 (hg17) chr3: 46,655,456-46,947,493 , GRCh37 (hg19) chr3: 46,680,452-46,972,489 , GRCh38 chr3: 46,638,962-46,930,999 PRSS46, CCDC12, 8 more genes
esv2759147copy number variation1estd1human GRCh38 chr3: 46,638,962-46,930,999 , GRCh37 (hg19) chr3: 46,680,452-46,972,489 , NCBI35 (hg17) chr3: 46,655,456-46,947,493 PRSS46, CCDC12, 8 more genes
esv2755378copy number variation1estd55human NCBI35 (hg17) chr3: 109,991-83,520,768 , GRCh37 (hg19) chr3: 134,991-83,438,078 , GRCh38 chr3: 93,308-83,388,927 SNORD19B, MIR885, 612 more genes
nsv915922copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr3: 46,743,108-46,984,809 , GRCh37 (hg19) chr3: 46,768,104-47,009,805 , GRCh38 chr3: 46,726,614-46,968,315 PRSS46, CCDC12, 5 more genes
nsv876755copy number variation1nstd71human NCBI36 (hg18) chr3: 46,870,113-47,036,187 , GRCh37 (hg19) chr3: 46,895,109-47,061,183 , GRCh38 chr3: 46,853,619-47,019,693 CCDC12, NBEAL2, 3 more genes
nsv876754copy number variation1nstd71human NCBI36 (hg18) chr3: 46,859,556-46,942,044 , GRCh37 (hg19) chr3: 46,884,552-46,967,040 , GRCh38 chr3: 46,843,062-46,925,550 CCDC12, MYL3, 1 more genes
nsv876753copy number variation1nstd71human NCBI36 (hg18) chr3: 46,859,556-46,932,302 , GRCh37 (hg19) chr3: 46,884,552-46,957,298 , GRCh38 chr3: 46,843,062-46,915,808 MYL3, PTH1R
nsv876752copy number variation1nstd71human NCBI36 (hg18) chr3: 46,854,835-46,942,044 , GRCh37 (hg19) chr3: 46,879,831-46,967,040 , GRCh38 chr3: 46,838,341-46,925,550 CCDC12, MYL3, 1 more genes
nsv590207copy number variation1nstd54human NCBI36 (hg18) chr3: 46,878,365-46,894,383 , GRCh37 (hg19) chr3: 46,903,361-46,919,379 , GRCh38 chr3: 46,861,871-46,877,889 MYL3, PTH1R
nsv590206copy number variation1nstd54human NCBI36 (hg18) chr3: 46,848,961-46,910,531 , GRCh37 (hg19) chr3: 46,873,957-46,935,527 , GRCh38 chr3: 46,832,467-46,894,037 PRSS42, MYL3, 1 more genes
nsv590205copy number variation1nstd54human NCBI36 (hg18) chr3: 46,827,683-46,904,550 , GRCh37 (hg19) chr3: 46,852,679-46,929,546 , GRCh38 chr3: 46,811,189-46,888,056 PRSS42, MYL3, 2 more genes
nsv590204copy number variation1nstd54human NCBI36 (hg18) chr3: 46,827,683-46,876,658 , GRCh37 (hg19) chr3: 46,852,679-46,901,654 , GRCh38 chr3: 46,811,189-46,860,164 PRSS42, MYL3, 1 more genes
nsv536558copy number variation1nstd54human NCBI36 (hg18) chr3: 46,681,575-46,999,760 , GRCh37 (hg19) chr3: 46,706,571-47,024,756 , GRCh38 chr3: 46,665,081-46,983,266 PRSS46, CCDC12, 9 more genes
nsv536554copy number variation1nstd54human NCBI36 (hg18) chr3: 46,627,347-46,961,582 , GRCh37 (hg19) chr3: 46,652,343-46,986,578 , GRCh38 chr3: 46,610,853-46,945,088 PRSS46, CCDC12, 8 more genes
nsv508915insertion1nstd49human NCBI35 (hg17) chr3: 46,830,843-46,929,967 , GRCh37 (hg19) chr3: 46,855,839-46,954,963 , GRCh38 chr3: 46,814,349-46,913,473 PRSS42, MYL3, 1 more genes
nsv491646copy number variation2nstd37humanPathogenic NCBI36 (hg18) chr3: 45,896,379-50,762,357 , GRCh37 (hg19) chr3: 45,921,375-50,787,353 , GRCh38 chr3: 45,879,883-50,749,922 PRSS46, MIR1226, 141 more genes

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