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Items: 1 to 20 of 4986

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4681134copy number variation2nstd102humanPathogenic, Likely benign GRCh37 chr2: 149,216,328-149,270,510 , GRCh38.p12 chr2: 148,458,759-148,512,941 MBD5
    nsv5673061copy number variation2nstd102humanPathogenic, Likely benign GRCh37 chr18: 48,604,616-48,604,837 , GRCh38.p12 chr18: 51,078,246-51,078,467 SMAD4
    nsv3906396copy number variation1nstd102humanLikely benign GRCh37 chr12: 61,060,570-61,949,046 , GRCh38.p12 chr12: 60,666,789-61,555,265 PGBD3P1
    nsv3879505copy number variation1nstd102humanLikely benign GRCh37 chr4: 91,797,748-92,473,294 , GRCh38.p12 chr4: 90,876,597-91,552,143 CCSER1
    nsv3924928copy number variation1nstd102humanLikely benign GRCh37 chr18: 63,909,629-64,457,524 , NCBI36 chr18: 62,060,609-62,608,504 , GRCh38 chr18: 66,242,392-66,790,287 CDH19
    nsv4729074copy number variation1nstd102humanLikely benign GRCh37 chr14: 33,463,166-33,998,038 , GRCh38.p12 chr14: 32,993,960-33,528,832 NPAS3
    nsv3908640copy number variation1nstd102humanLikely benign GRCh37 chr1: 105,427,063-105,928,237 , NCBI36 chr1: 105,228,586-105,729,760 , GRCh38 chr1: 104,884,441-105,385,615 LOC105378880
    nsv3913576copy number variation1nstd102humanLikely benign NCBI36 chr4: 64,351,877-64,826,147 , GRCh37.p13 chr4: 64,669,282-65,143,552 , GRCh38.p12 chr4: 63,803,564-64,277,834 TECRL
    nsv3902966copy number variation1nstd102humanLikely benign GRCh37 chr13: 55,521,443-55,988,184 , GRCh38.p12 chr13: 54,947,308-55,414,049 MIR5007
    nsv3892794copy number variation1nstd102humanLikely benign GRCh38 chr2: 137,028,226-137,470,344 , NCBI36 chr2: 137,502,266-137,944,384 , GRCh37 chr2: 137,785,796-138,227,914 THSD7B
    nsv3920333copy number variation1nstd102humanLikely benign GRCh37 chr13: 55,022,134-55,433,232 , NCBI36 chr13: 53,920,135-54,331,233 , GRCh38 chr13: 54,447,999-54,859,097 LOC105370213
    nsv3913714copy number variation1nstd102humanLikely benign NCBI36 chrX: 126,468,225-126,841,396 , GRCh37.p13 chrX: 126,640,544-127,013,715 , GRCh38.p12 chrX: 127,506,563-127,879,736 LOC100420320
    nsv3924328copy number variation1nstd102humanLikely benign NCBI36 chr6: 95,291,553-95,663,932 , GRCh37.p13 chr6: 95,234,832-95,607,211 , GRCh38.p12 chr6: 94,525,114-94,897,493 LOC105377901
    nsv3915201copy number variation1nstd102humanLikely benign NCBI36 chr13: 54,031,342-54,402,033 , GRCh37.p13 chr13: 55,133,341-55,504,032 , GRCh38.p12 chr13: 54,559,206-54,929,897 LOC105370213
    nsv3886466copy number variation1nstd102humanLikely benign GRCh37 chr5: 63,263,538-63,618,972 , GRCh38.p12 chr5: 63,967,711-64,323,145 RNF180
    nsv3915757copy number variation1nstd102humanLikely benign NCBI36 chrX: 115,967,232-116,322,263 , GRCh37.p13 chrX: 116,083,204-116,438,235 , GRCh38.p12 chrX: 116,949,236-117,304,272 SETP8
    nsv3893180copy number variation1nstd102humanLikely benign NCBI36 chr1: 188,825,774-189,180,317 , GRCh38 chr1: 190,590,021-190,944,564 , GRCh37 chr1: 190,559,151-190,913,694 LINC01720
    nsv3897046copy number variation1nstd102humanLikely benign GRCh37 chr11: 96,458,493-96,808,648 , GRCh38.p12 chr11: 96,587,493-96,937,648 AKTIPP3
    nsv3902773copy number variation1nstd102humanLikely benign GRCh38 chr2: 136,696,774-137,028,271 , NCBI36 chr2: 137,170,814-137,502,311 , GRCh37 chr2: 137,454,344-137,785,841 THSD7B
    nsv3920706copy number variation1nstd102humanLikely benign NCBI36 chr4: 161,567,500-161,898,485 , GRCh37.p13 chr4: 161,348,050-161,679,035 , GRCh38.p12 chr4: 160,426,898-160,757,883 LINC02477
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