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Items: 1 to 20 of 101

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5529144copy number variation1nstd206human GRCh38 chr19: 47,479,551-47,479,608 , GRCh37.p13 chr19: 47,982,808-47,982,865 KPTN
    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
    nsv4685764copy number variation1nstd102humannot provided GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460 SNAR-G1, IRF3, 453 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
    nsv4626594copy number variation1nstd183human GRCh37 chr19: 47,986,617-47,986,774 , GRCh38.p12 chr19: 47,483,360-47,483,517 NAPA-AS1, KPTN
    nsv4624453copy number variation1nstd183human GRCh37 chr19: 47,834,906-47,977,877 , GRCh38.p12 chr19: 47,331,649-47,474,620 C5AR2, SLC8A2, 3 more genes
    nsv4457518copy number variation1nstd102humanUncertain significance GRCh37 chr19: 47,785,567-48,178,258 , GRCh38.p12 chr19: 47,282,310-47,675,001 C5AR2, DHX34, 9 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
    nsv4272307copy number variation1nstd166human GRCh37.p13 chr19: 47,980,318-47,980,432 , GRCh38.p12 chr19: 47,477,061-47,477,175 KPTN
    nsv4264228copy number variation1nstd166human GRCh37.p13 chr19: 47,982,641-47,982,750 , GRCh38.p12 chr19: 47,479,384-47,479,493 KPTN
    nsv4255095copy number variation1nstd166human GRCh37.p13 chr19: 47,976,348-47,981,605 , GRCh38.p12 chr19: 47,473,091-47,478,348 KPTN
    nsv3956199copy number variation1nstd168human GRCh38 chr19: 47,448,362-47,510,988 , GRCh37.p13 chr19: 47,951,619-48,014,245 KPTN, NAPA-AS1, 2 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
    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
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