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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095480copy number variation4nstd102humanUncertain significance GRCh37 chr19: 39,904,727-42,931,301 , GRCh38.p12 chr19: 39,414,087-42,427,149 CYP2B6, EID2B, 140 more genes
    nsv7095205copy number variation2nstd102humanUncertain significance GRCh37 chr19: 39,205,089-40,913,839 , GRCh38.p12 chr19: 38,714,449-40,407,932 CCNP, NFKBIB, 81 more genes
    nsv7071361inversion1nstd229human GRCh38 chr19: 39,004,066-42,402,005 , GRCh37.p13 chr19: 39,494,706-42,906,157 RAB4B, RABAC1, 160 more genes
    nsv7068288inversion1nstd229human GRCh38 chr19: 39,023,970-42,945,419 , GRCh37.p13 chr19: 39,514,610-43,449,571 MIR4530, RNU6-195P, 178 more genes
    nsv7066709inversion1nstd229human GRCh38 chr19: 40,109,835-46,893,669 , GRCh37.p13 chr19: 40,615,742-47,396,926 LOC105372405, RNU6-611P, 305 more genes
    nsv7014085copy number variation1nstd229human GRCh38 chr19: 40,223,626-40,229,345 , GRCh37.p13 chr19: 40,729,533-40,735,252 CCNP, AKT2
    nsv7008831copy number variation1nstd229human GRCh38 chr19: 40,208,566-40,243,653 , GRCh37.p13 chr19: 40,714,473-40,749,560 CCNP, TTC9B, 2 more genes
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7006304copy number variation1nstd229human GRCh38 chr19: 40,217,175-40,226,587 , GRCh37.p13 chr19: 40,723,082-40,732,494 TTC9B, CCNP
    nsv7002183copy number variation1nstd229human GRCh38 chr19: 40,225,202-40,756,025 , GRCh37.p13 chr19: 40,731,109-41,261,930 RNU6-195P, LTBP4, 21 more genes
    nsv7000087copy number variation1nstd229human GRCh38 chr19: 39,937,301-40,261,900 , GRCh37.p13 chr19: 40,443,208-40,767,807 ZNF780A, CCNP, 10 more genes
    nsv6598416inversion1nstd223human GRCh38 chr19: 40,109,815-44,449,696 , GRCh37.p13 chr19: 40,615,722-44,953,884 , SERTAD1, 188 more genes
    nsv6521731copy number variation1nstd223human GRCh38 chr19: 40,223,625-40,229,348 , GRCh37.p13 chr19: 40,729,532-40,735,255 AKT2, CCNP
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv5977513insertion1nstd209human GRCh38 chr19: 40,227,178-40,227,178 , GRCh37.p13 chr19: 40,733,085-40,733,085 CCNP
    nsv5558284sequence alteration1nstd206human GRCh38 chr19: 40,171,920-40,325,062 , GRCh37.p13 chr19: 40,677,827-40,830,969 AKT2, MAP3K10, 6 more genes
    nsv5550170insertion1nstd206human GRCh38 chr19: 40,227,196-40,227,229 , GRCh37.p13 chr19: 40,733,103-40,733,136 CCNP
    nsv5287129copy number variation1nstd204human GRCh38.p13 chr19: 40,119,401-40,793,500 , GRCh37.p13 chr19: 40,625,308-41,299,405 CCNP, SHKBP1, 28 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
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