U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 44

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3919368copy number variation1nstd102humanPathogenic NCBI36 chr17: 15,704,477-20,556,000 , GRCh37.p13 chr17: 15,763,752-20,615,408 , GRCh38.p12 chr17: 15,860,438-20,712,095 TRPV2, CCDC144A, 196 more genes
    nsv3910522copy number variation1nstd102humanPathogenic GRCh37 chr17: 15,754,173-20,552,548 , GRCh38 chr17: 15,850,859-20,649,235 , NCBI36 chr17: 15,694,898-20,493,140 TRPV2, EEF1A1P43, 196 more genes
    nsv3917007copy number variation1nstd102humanPathogenic NCBI36 chr17: 15,573,932-20,354,156 , GRCh37 chr17: 15,633,207-20,413,564 , GRCh38 chr17: 15,729,893-20,510,251 TRPV2, LRRC75A, 193 more genes
    nsv3922067copy number variation1nstd102humanPathogenic NCBI36 chr17: 15,727,076-20,501,923 , GRCh38 chr17: 15,883,037-20,658,018 , GRCh37 chr17: 15,786,351-20,561,331 TRPV2, KRT16P4, 196 more genes
    nsv3922810copy number variation1nstd102humanPathogenic GRCh38 chr17: 15,883,037-20,620,700 , GRCh37 chr17: 15,786,351-20,524,013 , NCBI36 chr17: 15,727,076-20,464,605 TRPV2, SNORD49B, 194 more genes
    nsv3923405copy number variation1nstd102humanPathogenic NCBI36 chr17: 15,742,071-20,464,605 , GRCh38 chr17: 15,898,032-20,620,700 , GRCh37 chr17: 15,801,346-20,524,013 TRPV2, RPL21P121, 194 more genes
    nsv3908020copy number variation1nstd102humanPathogenic GRCh37 chr17: 15,745,315-20,261,191 , GRCh38.p12 chr17: 15,842,001-20,357,878 TRPV2, PEMT, 173 more genes
    nsv4675003copy number variation1nstd102humanPathogenic GRCh37 chr17: 15,632,431-18,726,389 , GRCh38.p12 chr17: 15,729,117-18,823,076 TRPV2, LLGL1, 127 more genes
    nsv3918054copy number variation1nstd102humanPathogenic GRCh38 chr17: 15,776,915-18,771,753 , NCBI36 chr17: 15,620,954-18,615,791 , GRCh37 chr17: 15,680,229-18,675,066 TRPV2, TBC1D27P, 121 more genes
    nsv4729738copy number variation1nstd102humanPathogenic GRCh37 chr17: 15,810,015-18,537,436 , GRCh38.p12 chr17: 15,906,701-18,634,123 TRPV2, UPF3AP1, 109 more genes
    nsv3923105copy number variation1nstd102humanPathogenic GRCh37 chr17: 15,855,385-18,266,133 , NCBI36 chr17: 15,796,110-18,206,858 , GRCh38 chr17: 15,952,071-18,362,819 TRPV2, NEK4P2, 89 more genes
    nsv3913316copy number variation1nstd102humanPathogenic NCBI36 chr17: 14,910,841-17,316,496 , GRCh38 chr17: 15,066,799-17,472,457 , GRCh37 chr17: 14,970,116-17,375,771 TRPV2, CDRT3, 86 more genes
    nsv3913412copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,021,199-18,266,133 , GRCh38 chr17: 16,117,885-18,362,819 , NCBI36 chr17: 15,961,924-18,206,858 TRPV2, EEF1A1P43, 83 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 TRPV2, MIR3185, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 TRPV2, P4HB, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 TRPV2, MIR21, 2366 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 TRPV2, SMURF2, 2366 more genes
    nsv3917939copy number variation1nstd102humanPathogenic GRCh38 chr17: 10,892,259-17,964,282 , NCBI36 chr17: 10,736,301-17,808,321 , GRCh37 chr17: 10,795,576-17,867,596 TRPV2, MIR744, 139 more genes
    nsv6315277copy number variation1nstd102humanPathogenic GRCh38 chr17: 11,915,997-17,892,664 , GRCh37.p13 chr17: 11,819,314-17,795,978 TRPV2, LINC02087, 135 more genes
    nsv3921507copy number variation1nstd102humanPathogenic GRCh38 chr17: 15,259,164-20,925,299 , GRCh37 chr17: 15,162,481-20,828,612 , NCBI36 chr17: 15,103,206-20,769,204 TRPV2, SCDP1, 232 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

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