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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097210copy number variation1nstd102humanUncertain significance GRCh37 chr3: 57,130,421-58,520,833 , GRCh38.p12 chr3: 57,096,393-58,535,106 LOC107984079, SLMAP, 37 more genes
    nsv7096473copy number variation1nstd102humanPathogenic GRCh37 chr3: 58,193,925-58,194,053 , GRCh38.p12 chr3: 58,208,198-58,208,326 DNASE1L3
    nsv7051968inversion1nstd229human GRCh38 chr3: 56,944,702-65,952,705 , GRCh37.p13 chr3: 56,978,730-65,938,380 ILF2P1, ARHGEF3-AS1, 115 more genes
    nsv7042731inversion1nstd229human GRCh38 chr3: 57,478,691-59,225,228 , GRCh37.p13 chr3: 57,464,418-59,210,954 ARF4-AS1, RNF7P1, 37 more genes
    nsv7039995inversion1nstd229human GRCh38 chr3: 57,602,974-58,277,050 , GRCh37.p13 chr3: 57,588,701-58,262,777 LOC105377104, ABHD6, 12 more genes
    nsv6709760copy number variation1nstd229human GRCh38 chr3: 58,075,498-58,356,448 , GRCh37.p13 chr3: 58,061,225-58,342,175 PXK, HTD2, 7 more genes
    nsv6709357copy number variation1nstd229human GRCh38 chr3: 58,078,101-58,393,500 , GRCh37.p13 chr3: 58,063,828-58,379,227 FLNB-AS1, LOC105377106, 7 more genes
    nsv6702742copy number variation1nstd229human GRCh38 chr3: 58,008,901-58,237,400 , GRCh37.p13 chr3: 57,994,628-58,223,127 FLNB-AS1, DNASE1L3, 3 more genes
    nsv6629052copy number variation1nstd224human GRCh37 chr3: 57,945,243-58,355,183 , GRCh38.p12 chr3: 57,959,516-58,369,456 FLNB, RPP14, 8 more genes
    nsv6551909inversion1nstd223human GRCh38 chr3: 57,602,973-58,277,049 , GRCh37.p13 chr3: 57,588,700-58,262,776 PDHA1P1, PPIAP16, 12 more genes
    nsv6542497inversion1nstd223human GRCh38 chr3: 58,202,341-58,202,866 , GRCh37.p13 chr3: 58,188,068-58,188,593 DNASE1L3
    nsv6355651copy number variation1nstd223human GRCh38 chr3: 58,203,698-58,203,905 , GRCh37.p13 chr3: 58,189,425-58,189,632 DNASE1L3
    nsv6311882copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 58,183,528-58,194,053 , GRCh38.p12 chr3: 58,197,801-58,208,326 DNASE1L3
    nsv6135018copy number variation1nstd213human GRCh37 chr3: 56,590,000-58,400,001 , GRCh38.p12 chr3: 56,555,972-58,414,274 ARF4, DNASE1L3, 36 more genes
    nsv5970656inversion1nstd209human GRCh38 chr3: 57,602,971-58,277,049 , GRCh37.p13 chr3: 57,588,698-58,262,776 DNASE1L3, FLNB, 12 more genes
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5438406copy number variation1nstd206human GRCh38 chr3: 58,209,889-58,210,015 , GRCh37.p13 chr3: 58,195,616-58,195,742 DNASE1L3
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4911556copy number variation1nstd200human GRCh38 chr3: 58,203,700-58,203,905 , GRCh37.p13 chr3: 58,189,427-58,189,632 DNASE1L3
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
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