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Items: 12

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    Number of Variants: 12

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv891485copy number variation111nstd71human NCBI36 chr8: 137,747,933-137,932,941 , GRCh37.p13 chr8: 137,678,751-137,863,759 , GRCh38.p12 chr8: 136,666,508-136,851,516 LINC02055
    nsv890817copy number variation29nstd71human NCBI36 chr8: 39,421,344-39,509,376 , GRCh37.p13 chr8: 39,302,187-39,390,219 , GRCh38.p12 chr8: 39,444,668-39,532,700 ADAM3A
    nsv882401copy number variation15nstd71human NCBI36 chr5: 97,073,409-97,127,572 , GRCh37.p13 chr5: 97,047,653-97,101,816 , GRCh38.p12 chr5: 97,711,949-97,766,112 LOC391813
    nsv884822copy number variation2547nstd71human NCBI36 chr6: 32,560,168-32,593,470 , GRCh37.p13 chr6: 32,452,190-32,485,492 , GRCh38.p12 chr6: 32,484,413-32,517,715 HLA-DRB5
    nsv885334copy number variation36nstd71human NCBI36 chr6: 32,632,659-32,647,375 , GRCh37.p13 chr6: 32,524,681-32,539,397 , GRCh38.p12 chr6: 32,556,904-32,571,620 HLA-DRB6
    nsv881673copy number variation95nstd71human NCBI36 chr5: 9,953,083-9,981,862 , GRCh37.p13 chr5: 9,900,083-9,928,862 , GRCh38.p12 chr5: 9,899,971-9,928,750 LOC107986405, LINC02112
    nsv879310copy number variation1929nstd71human NCBI36 chr4: 69,076,346-69,179,871 , GRCh37.p13 chr4: 69,393,751-69,497,276 , GRCh38.p12 chr4: 68,528,033-68,631,558 LOC100422402, LOC100132651, 2 more genes
    nsv898369copy number variation2nstd71human NCBI36 chr11: 106,463,514-106,948,630 , GRCh37.p13 chr11: 106,958,304-107,443,420 , GRCh38.p12 chr11: 107,087,578-107,572,694 SMARCE1P1, LOC105369477, 3 more genes
    nsv901580copy number variation1nstd71human NCBI36 chr14: 29,880,418-29,984,418 , GRCh37.p13 chr14: 30,810,667-30,914,667 , GRCh38.p12 chr14: 30,341,461-30,445,461 G2E3-AS1, LOC112267868, 1 more genes
    nsv871709copy number variation27nstd71human NCBI36 chr1: 103,904,580-103,966,748 , GRCh37.p13 chr1: 104,103,057-104,165,225 , GRCh38.p12 chr1: 103,560,435-103,622,603 AMY2B, ACTG1P4, 1 more genes
    nsv873943copy number variation269nstd71human NCBI36 chr2: 41,083,802-41,109,046 , GRCh37.p13 chr2: 41,230,298-41,255,542 , GRCh38.p12 chr2: 41,003,158-41,028,402 0
    nsv901581copy number variation1nstd71human NCBI36 chr14: 30,048,496-30,655,040 , GRCh37.p13 chr14: 30,978,745-31,585,289 , GRCh38.p12 chr14: 30,509,539-31,116,083 COCH, RPL21P5, 16 more genes
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