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Items: 1 to 20 of 91

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5933499copy number variation1nstd209human GRCh38 chr19: 45,073,531-45,073,602 , GRCh37.p13 chr19: 45,576,789-45,576,860 ZNF296
    nsv5929013copy number variation1nstd209human GRCh38 chr19: 45,073,984-45,074,322 , GRCh37.p13 chr19: 45,577,242-45,577,580 ZNF296, GEMIN7
    nsv5521357copy number variation1nstd206human GRCh38 chr19: 45,073,532-45,073,603 , GRCh37.p13 chr19: 45,576,790-45,576,861 ZNF296
    nsv5020665copy number variation1nstd200human GRCh38 chr19: 45,075,182-45,075,296 , GRCh37.p13 chr19: 45,578,440-45,578,554 ZNF296, GEMIN7
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4676350copy number variation1nstd102humanUncertain significance GRCh37 chr19: 45,531,056-48,174,177 , GRCh38.p12 chr19: 45,027,798-47,670,920 NKPD1, IGFL1, 112 more genes
    nsv4631923copy number variation1nstd183human GRCh37 chr19: 45,525,537-45,768,917 , GRCh38.p12 chr19: 45,022,279-45,265,659 BLOC1S3, CLASRP, 13 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
    nsv4270144copy number variation1nstd166human GRCh37.p13 chr19: 45,554,636-45,590,509 , GRCh38.p12 chr19: 45,051,378-45,087,251 GEMIN7, GEMIN7-AS1, 2 more genes
    nsv4265441copy number variation1nstd166human GRCh37.p13 chr19: 45,576,790-45,576,861 , GRCh38.p12 chr19: 45,073,532-45,073,603 ZNF296
    nsv3924836copy number variation1nstd102humanPathogenic NCBI36 chr19: 50,166,517-53,452,471 , GRCh37 chr19: 45,474,677-48,760,659 , GRCh38 chr19: 44,971,420-48,257,402 IGFL1P1, LOC105372426, 145 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3904541copy number variation1nstd102humanUncertain significance GRCh37 chr19: 45,284,576-45,978,239 , GRCh38.p12 chr19: 44,781,319-45,474,981 MIR6088, LOC100420902, 33 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3900788copy number variation1nstd102humanBenign GRCh37 chr19: 45,338,895-45,618,902 , GRCh38.p12 chr19: 44,835,638-45,115,644 APOC2, APOC1, 14 more genes
    nsv3891669copy number variation1nstd102humanPathogenic GRCh37 chr19: 43,013,365-47,241,534 , GRCh38.p12 chr19: 42,509,213-46,738,277 MIR320E, BCL3, 189 more genes
    nsv3890841copy number variation1nstd102humanUncertain significance GRCh37 chr19: 44,300,416-45,639,540 , GRCh38.p12 chr19: 43,796,264-45,136,282 ZNF225, ZNF296, 57 more genes
    nsv3167210copy number variation1nstd151human GRCh37 chr19: 45,555,326-45,579,125 , GRCh38.p12 chr19: 45,052,068-45,075,867 CLASRP, GEMIN7, 1 more genes
    nsv3165343copy number variation1nstd151human GRCh37 chr19: 45,572,321-45,579,636 , GRCh38.p12 chr19: 45,069,063-45,076,378 CLASRP, ZNF296, 1 more genes
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