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 204

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6313317copy number variation1nstd102humanPathogenic GRCh37 chrX: 13,753,081-13,765,093 , GRCh38.p12 chrX: 13,734,962-13,746,974 TRAPPC2, OFD1
    nsv3882373copy number variation1nstd102humanPathogenic GRCh38 chrX: 13,735,052-13,744,539 , GRCh37 chrX: 13,753,171-13,762,658 TRAPPC2, OFD1
    nsv997147copy number variation1nstd45humanPathogenic GRCh37 chrX: 13,730,361-13,752,754 , GRCh38.p12 chrX: 13,712,242-13,734,635 TRAPPC2, OFD1
    nsv6313038copy number variation1nstd102humanUncertain significance GRCh37 chrX: 13,732,526-13,762,658 , GRCh38.p12 chrX: 13,714,407-13,744,539 TRAPPC2, OFD1
    nsv4453964copy number variation1nstd102humanUncertain significance GRCh38 chrX: 13,734,961-13,736,697 , GRCh37 chrX: 13,753,080-13,754,816 TRAPPC2, OFD1
    nsv3876272copy number variation1nstd102humanPathogenic GRCh38 chrX: 13,735,052-13,769,128 , GRCh37.p13 chrX: 13,753,171-13,787,247 TRAPPC2, GPM6B, 1 more genes
    nsv997093copy number variation1nstd45humanPathogenic GRCh37 chrX: 13,752,832-13,787,480 , GRCh38.p12 chrX: 13,734,713-13,769,361 TRAPPC2, GPM6B, 1 more genes
    nsv4682997copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chrX: 13,753,185-13,787,232 , GRCh38.p12 chrX: 13,735,066-13,769,113 TRAPPC2, GPM6B, 1 more genes
    nsv7097992copy number variation1nstd102humanUncertain significance GRCh37 chrX: 13,734,103-13,787,227 , GRCh38.p12 chrX: 13,715,984-13,769,108 TRAPPC2, OFD1, 1 more genes
    nsv3904162copy number variation1nstd102humanPathogenic GRCh38 chrX: 10,001-156,030,895 , GRCh37 chrX: 60,001-155,260,560 , NCBI36 chrX: 1-154,913,754 TRAPPC2, NANOGNBP3, 2154 more genes
    nsv3913255copy number variation2nstd102humanPathogenic NCBI36 chrX: 701-154,913,754 , GRCh37.p13 chrX: 60,701-155,260,560 , GRCh38.p12 chrX: 10,701-156,030,895 TRAPPC2, NHS-AS1, 2154 more genes
    nsv3907094copy number variation4nstd102humanPathogenic GRCh38 chrX: 10,679-156,022,206 , GRCh37 chrX: 60,679-155,251,871 , NCBI36 chrX: 679-154,905,065 TRAPPC2, GPR119, 2153 more genes
    nsv3878553copy number variation2nstd102humanPathogenic GRCh37 chrX: 60,262-155,245,765 , GRCh38.p12 chrX: 10,262-156,016,100 TRAPPC2, H2AB2, 2152 more genes
    nsv3898149copy number variation1nstd102humanPathogenic GRCh38 chrX: 20,297-156,026,127 , NCBI36 chrX: 10,297-154,908,986 , GRCh37 chrX: 70,297-155,255,792 TRAPPC2, OR3B1P, 2154 more genes
    nsv3877395copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,839 , GRCh38.p12 chrX: 21,267-156,026,174 TRAPPC2, ARMCX2, 2154 more genes
    nsv3884935copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,792 , GRCh38.p12 chrX: 21,267-156,026,127 TRAPPC2, NDUFB11, 2154 more genes
    nsv3903061copy number variation1nstd102humanPathogenic NCBI36 chrX: 679-154,896,026 , GRCh38 chrX: 10,679-156,013,167 , GRCh37 chrX: 60,679-155,242,832 TRAPPC2, SLC38A5, 2152 more genes
    nsv3885865copy number variation1nstd102humanPathogenic GRCh37 chrX: 70,297-155,246,585 , GRCh38.p12 chrX: 20,297-156,016,920 TRAPPC2, MIR1277, 2152 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 TRAPPC2, LOC105373176, 2151 more genes
    nsv3907545copy number variation1nstd102humanPathogenic GRCh37 chrX: 64,245-155,228,958 , NCBI36 chrX: 4,245-154,882,152 , GRCh38 chrX: 14,245-155,999,293 TRAPPC2, TMEM30BP1, 2151 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