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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978990inversion1nstd209human GRCh38 chr13: 19,387,175-24,442,537 , GRCh37.p13 chr13: 19,961,315-25,016,675 , PARP4, 111 more genes
    nsv5969193inversion1nstd209human GRCh38 chr13: 19,344,229-24,542,503 , GRCh37.p13 chr13: 19,918,369-25,116,641 , PARP4, 117 more genes
    nsv5930119copy number variation1nstd209human GRCh38 chr13: 19,425,704-24,953,999 , GRCh37.p13 chr13: 19,999,844-25,528,137 , LOC105370102, 128 more genes
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5561828sequence alteration1nstd206human GRCh38 chr13: 20,147,502-20,285,066 , GRCh37.p13 chr13: 20,721,641-20,859,205 GJA3, GJB2, 3 more genes
    nsv5501654copy number variation1nstd206human GRCh38 chr13: 20,124,106-20,285,000 , GRCh37.p13 chr13: 20,698,245-20,859,139 GJA3, GJB6, 3 more genes
    nsv5302163copy number variation1nstd204human GRCh38.p13 chr13: 20,124,774-20,193,432 , GRCh37.p13 chr13: 20,698,913-20,767,571 LOC107984553, GJA3, 2 more genes
    nsv5030395inversion1nstd200human GRCh38 chr13: 19,051,676-20,424,293 , GRCh37.p13 chr13: 19,625,816-20,998,432 CYCSP32, ESRRAP1, 35 more genes
    nsv5004362copy number variation1nstd200human GRCh38 chr13: 19,736,397-20,507,810 , GRCh37.p13 chr13: 20,310,537-21,081,949 KRR1P1, LINC01072, 14 more genes
    nsv4885308inversion1nstd200human GRCh37 chr13: 19,625,812-20,998,432 , GRCh38.p12 chr13: 19,051,672-20,424,293 GJB2, TPTE2-AS1, 35 more genes
    nsv4730392copy number variation1nstd199human GRCh37 chr13: 20,760,233-20,760,287 , GRCh38.p12 chr13: 20,186,094-20,186,148 GJB2, LOC107984553
    nsv4683415copy number variation1nstd102humanUncertain significance GRCh37 chr13: 20,716,100-21,398,980 , GRCh38.p12 chr13: 20,141,961-20,824,841 GJB6, EEF1AKMT1, 14 more genes
    nsv4675707copy number variation1nstd102humanUncertain significance GRCh37 chr13: 19,436,286-20,886,867 , GRCh38.p12 chr13: 18,862,146-20,312,728 PHF2P1, MRPL3P1, 43 more genes
    nsv4675550copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-24,970,361 , GRCh38.p12 chr13: 18,862,146-24,396,223 MRPL57, TATDN2P3, 129 more genes
    nsv4675255copy number variation1nstd102humanPathogenic GRCh37 chr13: 20,668,070-23,029,230 , GRCh38.p12 chr13: 20,093,931-22,455,091 RPSAP54, SLC35E1P1, 52 more genes
    nsv4675068copy number variation1nstd102humanUncertain significance GRCh37 chr13: 20,722,953-20,855,764 , GRCh38.p12 chr13: 20,148,814-20,281,625 GJB6, PPIAP28, 3 more genes
    nsv4529309copy number variation1nstd166human GRCh37.p13 chr13: 20,691,499-21,088,000 , GRCh38.p12 chr13: 20,117,360-20,513,861 GJA3, GJB2, 7 more genes
    nsv4457197copy number variation1nstd102humanPathogenic GRCh37 chr13: 20,069,228-27,474,401 , GRCh38.p12 chr13: 19,495,088-26,900,264 ZDHHC20, ANKRD20A10P, 154 more genes
    nsv4457034copy number variation1nstd102humanUncertain significance GRCh37 chr13: 20,705,241-21,089,219 , GRCh38.p12 chr13: 20,131,102-20,515,080 PPIAP28, LOC105370102, 6 more genes
    nsv4456640copy number variation1nstd102humanPathogenic GRCh37 chr13: 20,562,171-22,993,375 , GRCh38.p12 chr13: 19,988,031-22,419,236 RANP8, PPIAP28, 53 more genes
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