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 138

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098791copy number variation1nstd102humanPathogenic GRCh37 chr17: 55,442,363-56,309,063 , GRCh38.p12 chr17: 57,365,002-58,231,702 MKS1, OR4D2, 21 more genes
    nsv7058620inversion1nstd229human GRCh38 chr17: 57,249,365-57,569,630 , GRCh37.p13 chr17: 55,326,726-55,646,991 LOC101927557, MSI2, 2 more genes
    nsv6994267copy number variation1nstd229human GRCh38 chr17: 57,512,501-57,525,400 , GRCh37.p13 chr17: 55,589,862-55,602,761 MSI2, LOC101927557
    nsv6987200copy number variation1nstd229human GRCh38 chr17: 57,495,701-57,648,700 , GRCh37.p13 chr17: 55,573,062-55,726,061 LOC101927557, LOC107984993, 3 more genes
    nsv6637714copy number variation1nstd102humanUncertain significance GRCh37 chr17: 55,356,209-55,680,113 , GRCh38.p12 chr17: 57,278,848-57,602,752 MSI2, LOC101927539, 2 more genes
    nsv6637352copy number variation1nstd102humanUncertain significance GRCh37 chr17: 55,425,668-55,856,050 , GRCh38.p12 chr17: 57,348,307-57,778,689 LOC101927539, LOC107984993, 5 more genes
    nsv6634423copy number variation1nstd102humanPathogenic GRCh37 chr17: 55,043,662-56,728,123 , GRCh38.p12 chr17: 56,966,301-58,650,762 RNU7-134P, DYNLL2-DT, 42 more genes
    nsv6520976copy number variation1nstd223human GRCh38 chr17: 57,495,667-57,648,705 , GRCh37.p13 chr17: 55,573,028-55,726,066 LOC101927557, LOC107984993, 3 more genes
    nsv6310393copy number variation1nstd102humanUncertain significance GRCh37 chr17: 54,671,585-59,938,900 , GRCh38.p12 chr17: 56,594,224-61,861,539 RNF43, LOC107985048, 132 more genes
    nsv6133317copy number variation1nstd213human GRCh37 chr17: 55,470,000-55,650,001 , GRCh38.p12 chr17: 57,392,639-57,572,640 MSI2, LOC101927557, 1 more genes
    nsv6133316copy number variation1nstd213human GRCh37 chr17: 53,930,000-62,410,001 , GRCh38.p12 chr17: 55,852,639-64,332,641 CA4, CD79B, 208 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv4679207copy number variation1nstd189human GRCh37.p13 chr17: 55,459,753-55,983,187 , GRCh38.p12 chr17: 57,382,392-57,905,826 MRPS23, MSI2, 8 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv3920623copy number variation1nstd102humanPathogenic GRCh37 chr17: 54,760,866-56,162,300 , NCBI36 chr17: 52,115,865-53,517,299 , GRCh38 chr17: 56,683,505-58,084,939 C17orf67, CUEDC1, 28 more genes
    nsv3917224copy number variation1nstd102humanPathogenic GRCh38 chr17: 56,958,745-58,171,125 , NCBI36 chr17: 52,391,105-53,603,485 , GRCh37 chr17: 55,036,106-56,248,486 MRPS23, MSX2P1, 24 more genes
    nsv3914957copy number variation1nstd102humanPathogenic GRCh37 chr17: 55,496,167-57,812,825 , GRCh38 chr17: 57,418,806-59,735,464 , NCBI36 chr17: 52,851,166-55,167,607 CLTC, LOC101927557, 67 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 PRPSAP1, CACNG1, 1350 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