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Items: 1 to 20 of 235

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv5966806insertion1nstd209human GRCh38 chr4: 24,550,089-24,550,089 , GRCh37.p13 chr4: 24,551,712-24,551,712 DHX15
    nsv5964134insertion1nstd209human GRCh38 chr4: 24,574,205-24,574,205 , GRCh37.p13 chr4: 24,575,828-24,575,828 DHX15
    nsv5906067copy number variation1nstd209human GRCh38 chr4: 22,920,705-27,042,181 , GRCh37.p13 chr4: 22,922,328-27,043,803 , SEPSECS, 49 more genes
    nsv5888349copy number variation1nstd209human GRCh38 chr4: 24,535,907-24,536,560 , GRCh37.p13 chr4: 24,537,530-24,538,183 DHX15
    nsv5839228copy number variation2nstd209human GRCh38 chr4: 24,553,274-24,554,387 , GRCh37.p13 chr4: 24,554,897-24,556,010 DHX15
    nsv5724591mobile element insertion1nstd211human GRCh38 chr4: 24,562,407-24,562,407 , GRCh37.p13 chr4: 24,564,030-24,564,030 DHX15, RN7SL16P
    nsv5690281mobile element insertion1nstd211human GRCh38 chr4: 24,543,782-24,543,782 , GRCh37.p13 chr4: 24,545,405-24,545,405 DHX15
    nsv5556828mobile element insertion1nstd206human GRCh38 chr4: 24,562,422-24,562,458 , GRCh37.p13 chr4: 24,564,045-24,564,081 RN7SL16P, DHX15
    nsv5545914insertion1nstd206human GRCh38 chr4: 24,547,954-24,547,960 , GRCh37.p13 chr4: 24,549,577-24,549,583 DHX15
    nsv5434279copy number variation1nstd206human GRCh38 chr4: 24,529,132-24,529,220 , GRCh37.p13 chr4: 24,530,755-24,530,843 DHX15
    nsv5352673translocation1nstd200human GRCh38 chr4: 24,557,568-24,557,568 , GRCh38 chr4: 24,557,764-24,557,764 , GRCh37.p13 chr4: 24,559,387-24,559,387 , GRCh37.p13 chr4: 24,559,191-24,559,191 DHX15
    nsv5352672translocation1nstd200human GRCh38 chr4: 24,550,861-24,550,861 , GRCh38 chr4: 24,550,754-24,550,754 , GRCh37.p13 chr4: 24,552,484-24,552,484 , GRCh37.p13 chr4: 24,552,377-24,552,377 DHX15
    nsv5352669translocation1nstd200human GRCh38 chr4: 24,558,403-24,558,403 , GRCh38 chr4: 24,440,186-24,440,186 , GRCh37.p13 chr4: 24,560,026-24,560,026 , GRCh37.p13 chr4: 24,441,809-24,441,809 PPARGC1A, DHX15
    nsv5329602translocation1nstd200human GRCh37 chr4: 24,441,809-24,441,809 , GRCh37 chr4: 24,560,026-24,560,026 , GRCh38.p12 chr4: 24,440,186-24,440,186 , GRCh38.p12 chr4: 24,558,403-24,558,403 PPARGC1A, DHX15
    nsv5096504mobile element insertion1nstd203human GRCh38 chr4: 24,543,770-24,543,782 , GRCh37.p13 chr4: 24,545,393-24,545,405 DHX15
    nsv5093856mobile element insertion1nstd203human GRCh38 chr4: 24,550,094-24,550,123 , GRCh37.p13 chr4: 24,551,717-24,551,746 DHX15
    nsv5089720mobile element insertion1nstd203human GRCh38 chr4: 24,574,205-24,574,228 , GRCh37.p13 chr4: 24,575,828-24,575,851 DHX15
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv4925379copy number variation1nstd200human GRCh38 chr4: 24,409,942-24,692,090 , GRCh37.p13 chr4: 24,411,565-24,693,713 MIR573, DHX15, 4 more genes
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