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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093376copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 156,786,013-162,945,369 , GRCh38.p12 chr5: 157,359,005-163,518,363 ADRA1B, CCNG1, 81 more genes
    nsv7057344inversion1nstd229human GRCh38 chr5: 158,420,376-160,356,139 , GRCh37.p13 chr5: 157,847,384-159,783,146 LINC01845, TTC1, 27 more genes
    nsv7054438inversion1nstd229human GRCh38 chr5: 158,806,124-160,433,845 , GRCh37.p13 chr5: 158,233,132-159,860,852 LINC01845, TTC1, 30 more genes
    nsv7043766inversion1nstd229human GRCh38 chr5: 158,447,259-160,356,138 , GRCh37.p13 chr5: 157,874,267-159,783,145 ADRA1B, LOC105377687, 27 more genes
    nsv6794984copy number variation1nstd229human GRCh38 chr5: 159,275,371-163,261,193 , GRCh37.p13 chr5: 158,702,379-162,688,199 LOC105377685, CCNJL, 45 more genes
    nsv6790999copy number variation1nstd229human GRCh38 chr5: 160,055,547-160,056,783 , GRCh37.p13 chr5: 159,482,554-159,483,790 PWWP2A, TTC1
    nsv6790045copy number variation1nstd229human GRCh38 chr5: 160,110,460-160,110,966 , GRCh37.p13 chr5: 159,537,467-159,537,973 PWWP2A
    nsv6788943copy number variation1nstd229human GRCh38 chr5: 160,099,519-160,109,831 , GRCh37.p13 chr5: 159,526,526-159,536,838 PWWP2A
    nsv6787722copy number variation1nstd229human GRCh38 chr5: 160,076,999-160,077,540 , GRCh37.p13 chr5: 159,504,006-159,504,547 PWWP2A
    nsv6784690copy number variation1nstd229human GRCh38 chr5: 160,067,541-160,075,631 , GRCh37.p13 chr5: 159,494,548-159,502,638 PWWP2A
    nsv6781237copy number variation1nstd229human GRCh38 chr5: 160,080,001-160,394,000 , GRCh37.p13 chr5: 159,507,008-159,821,007 FABP6-AS1, C1QTNF2, 7 more genes
    nsv6780685copy number variation1nstd229human GRCh38 chr5: 160,098,836-160,102,117 , GRCh37.p13 chr5: 159,525,843-159,529,124 PWWP2A
    nsv6636891copy number variation1nstd102humanPathogenic GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790 EFCAB9, LOC112267936, 287 more genes
    nsv6636858copy number variation1nstd102humanUncertain significance GRCh37 chr5: 159,535,230-161,656,766 , GRCh38.p12 chr5: 160,108,223-162,229,760 MIR146A, SNRPEP1, 23 more genes
    nsv6574346inversion1nstd223human GRCh38 chr5: 160,095,032-160,095,712 , GRCh37.p13 chr5: 159,522,039-159,522,719 PWWP2A
    nsv6569917inversion1nstd223human GRCh38 chr5: 160,050,252-160,050,773 , GRCh37.p13 chr5: 159,477,259-159,477,780 TTC1, PWWP2A
    nsv6560533inversion1nstd223human GRCh38 chr5: 160,099,766-160,100,179 , GRCh37.p13 chr5: 159,526,773-159,527,186 PWWP2A
    nsv6560496inversion1nstd223human GRCh38 chr5: 160,097,551-160,097,997 , GRCh37.p13 chr5: 159,524,558-159,525,004 PWWP2A
    nsv6399997copy number variation1nstd223human GRCh38 chr5: 160,118,401-160,118,900 , GRCh37.p13 chr5: 159,545,408-159,545,907 PWWP2A
    nsv6396692copy number variation1nstd223human GRCh38 chr5: 160,055,545-160,056,780 , GRCh37.p13 chr5: 159,482,552-159,483,787 PWWP2A, TTC1
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