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Items: 1 to 20 of 93

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5293275copy number variation1nstd204human GRCh38.p13 chr19: 47,049,201-47,476,100 , GRCh37.p13 chr19: 47,552,459-47,979,357 , ZC3H4, 12 more genes
    nsv5287634copy number variation1nstd204human GRCh38.p13 chr19: 47,201,401-47,396,100 , GRCh37.p13 chr19: 47,704,658-47,899,357 , DHX34, 8 more genes
    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
    nsv4676254copy number variation1nstd102humanUncertain significance GRCh37 chr19: 47,331,662-48,234,260 , GRCh38.p12 chr19: 46,828,405-47,731,003 AP2S1, BICRA, 22 more genes
    nsv4625235copy number variation1nstd183human GRCh37 chr19: 47,763,285-47,810,913 , GRCh38.p12 chr19: 47,260,028-47,307,656 , INAFM1, 1 more genes
    nsv4620362copy number variation1nstd183human GRCh37 chr19: 47,518,852-47,908,504 , GRCh38.p12 chr19: 47,015,595-47,405,247 , SAE1, 12 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
    nsv4350827copy number variation1nstd102humanPathogenic GRCh37 chr19: 47,036,361-48,525,536 , GRCh38.p12 chr19: 46,533,104-48,022,279 LINC01595, SNAR-A13, 59 more genes
    nsv4321864inversion1nstd166human GRCh37.p13 chr19: 46,657,897-51,634,775 , GRCh38.p12 chr19: 46,154,640-51,131,518 , C5AR1, 288 more genes
    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
    nsv3923488copy number variation1nstd102humanUncertain significance NCBI36 chr19: 52,232,982-52,520,971 , GRCh37.p13 chr19: 47,541,142-47,829,131 , GRCh38.p12 chr19: 47,037,884-47,325,874 C5AR1, MIR3190, 8 more genes
    nsv3918983copy number variation1nstd102humanPathogenic GRCh38 chr19: 46,658,791-49,050,450 , GRCh37 chr19: 47,162,048-49,553,707 , NCBI36 chr19: 51,853,888-54,245,519 LOC105372432, FTL, 121 more genes
    nsv3911937copy number variation1nstd102humanLikely benign GRCh37 chr19: 47,756,887-48,247,971 , NCBI36 chr19: 52,448,727-52,939,783 , GRCh38 chr19: 47,253,630-47,744,714 RN7SL322P, NAPA, 13 more genes
    nsv3910109copy number variation1nstd102humanPathogenic GRCh38 chr19: 46,458,122-47,683,579 , GRCh37 chr19: 46,961,379-48,186,836 , NCBI36 chr19: 51,653,219-52,878,648 FKRP, GNG8, 38 more genes
    nsv3909504copy number variation1nstd102humanUncertain significance GRCh37 chr19: 47,228,251-47,867,279 , GRCh38.p12 chr19: 46,724,994-47,364,022 CCDC9, TMEM160, 17 more genes
    nsv3907578copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 47,450,549-47,880,338 , GRCh38.p12 chr19: 46,947,292-47,377,081 C5AR1, ARHGAP35, 11 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
    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
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