U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 74

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7064705inversion1nstd229human GRCh38 chr19: 9,214,745-9,235,146 , GRCh37.p13 chr19: 9,325,421-9,345,822 OR7D1P, OR7D4, 1 more genes
    nsv7012246copy number variation1nstd229human GRCh38 chr19: 9,202,317-9,299,718 , GRCh37.p13 chr19: 9,312,993-9,410,394 OR7E24, OR7D4, 7 more genes
    nsv7011121copy number variation1nstd229human GRCh38 chr19: 7,159,006-9,938,147 , GRCh37.p13 chr19: 7,159,017-10,048,823 , OR7G1, 117 more genes
    nsv6596198inversion1nstd223human GRCh38 chr19: 9,191,684-9,261,386 , GRCh37.p13 chr19: 9,302,360-9,372,062 OR7E16P, OR7E25P, 5 more genes
    nsv6530391copy number variation1nstd223human GRCh38 chr19: 9,198,359-9,247,331 , GRCh37.p13 chr19: 9,309,035-9,358,007 OR7D11P, OR7D4, 2 more genes
    nsv6523253copy number variation1nstd223human GRCh38 chr19: 9,161,601-9,259,100 , GRCh37.p13 chr19: 9,272,277-9,369,776 OR7E25P, ZNF317, 8 more genes
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133479copy number variation1nstd213human GRCh37 chr19: 7,400,000-13,280,001 , GRCh38.p12 chr19: 7,335,095-13,169,187 , ACP5, 299 more genes
    nsv4729955copy number variation1nstd102humanLikely benign GRCh37 chr19: 9,245,167-9,465,565 , GRCh38.p12 chr19: 9,134,491-9,354,889 ZNF699, ZNF559-ZNF177, 14 more genes
    nsv4729799copy number variation1nstd102humanUncertain significance GRCh37 chr19: 8,518,395-10,053,298 , GRCh38.p12 chr19: 8,453,511-9,942,622 ZNF426-DT, ADAMTS10, 61 more genes
    nsv4436244complex substitution1nstd102humanUncertain significance GRCh38.p12 chr19: 8,891,157-9,974,378 , GRCh37 chr19: 9,001,833-10,085,054 PIN1, UBE2L4, 51 more genes
    nsv3920616copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 8,802,823-13,303,041 , GRCh37 chr19: 8,941,823-13,442,041 , GRCh38 chr19: 8,831,147-13,331,227 ACP5, GET3, 236 more genes
    nsv3914351copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555 SEMA6B, RANBP3-DT, 299 more genes
    nsv3907034copy number variation1nstd102humanLikely benign GRCh37 chr19: 8,905,057-9,606,461 , GRCh38.p12 chr19: 8,794,381-9,495,785 ZNF559-ZNF177, OR7E18P, 30 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
    nsv3890584copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,120,160-9,732,820 , GRCh38.p12 chr19: 3,120,162-9,622,144 PCP2, EIF1P6, 250 more genes
    nsv3888397copy number variation1nstd102humanLikely pathogenic GRCh38 chr19: 7,981,357-10,019,383 , GRCh37.p13 chr19: 8,046,241-10,130,059 ELAVL1, MYO1F, 80 more genes
    nsv3162685copy number variation1nstd151human GRCh37 chr19: 9,203,910-9,325,518 , GRCh38.p12 chr19: 9,093,234-9,214,842 OR7E25P, OR7G15P, 10 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center