U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from OMIM

Items: 1 to 20 of 233

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6638087insertion1nstd102humanUncertain significance GRCh37 chr11: 66,008,249-66,008,249 , GRCh38 chr11: 66,240,778-66,240,778 PACS1
    nsv6638085insertion1nstd102humanUncertain significance GRCh38 chr15: 76,431,158-76,431,158 , GRCh37 chr15: 76,723,499-76,723,499 SCAPER
    nsv6638084insertion1nstd102humanUncertain significance GRCh38 chr15: 51,686,717-51,686,717 , GRCh37 chr15: 51,978,914-51,978,914 SCG3
    nsv6638083insertion1nstd102humanUncertain significance GRCh38 chr9: 94,625,120-94,625,120 , GRCh37 chr9: 97,387,402-97,387,402 FBP1
    nsv6638082insertion1nstd102humanUncertain significance GRCh37 chr7: 78,997,174-78,997,174 , GRCh38 chr7: 79,367,858-79,367,858 MAGI2
    nsv6638081insertion1nstd102humanUncertain significance GRCh38 chr21: 37,632,245-37,632,245 , GRCh37 chr21: 39,004,547-39,004,547 KCNJ6
    nsv6638080insertion1nstd102humanUncertain significance GRCh37 chr18: 59,713,725-59,713,725 , GRCh38 chr18: 62,046,492-62,046,492 PIGN
    nsv6638078insertion1nstd102humanUncertain significance GRCh38 chr22: 26,601,647-26,601,647 , GRCh37 chr22: 26,997,611-26,997,611 CRYBB1
    nsv6638077insertion1nstd102humanUncertain significance GRCh37 chr5: 78,253,753-78,253,753 , GRCh38 chr5: 78,957,930-78,957,930 ARSB
    nsv6638076insertion1nstd102humanUncertain significance GRCh38 chr4: 150,372,755-150,372,755 , GRCh37 chr4: 151,293,907-151,293,907 LRBA
    nsv6638075insertion1nstd102humanUncertain significance GRCh38 chr4: 42,920,715-42,920,715 , GRCh37 chr4: 42,922,732-42,922,732 GRXCR1
    nsv6638062insertion1nstd102humanUncertain significance GRCh38 chr2: 15,379,421-15,379,421 , GRCh37 chr2: 15,519,545-15,519,545 NBAS
    nsv6638061insertion1nstd102humanUncertain significance GRCh37 chr3: 33,085,270-33,085,270 , GRCh38 chr3: 33,043,778-33,043,778 GLB1
    nsv6636185copy number variation1nstd102humanUncertain significance GRCh38 chr10: 51,553,704-51,553,764 , GRCh37 chr10: 53,313,464-53,313,524 PRKG1
    nsv6636183copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,111,845-138,112,038 , GRCh38 chr5: 138,776,156-138,776,349 CTNNA1
    nsv6636180copy number variation1nstd102humanUncertain significance GRCh38 chr2: 239,925,792-239,928,083 , GRCh37 chr2: 240,865,209-240,867,500 NDUFA10
    nsv6636161copy number variation1nstd102humanUncertain significance GRCh38 chr7: 147,347,421-147,347,480 , GRCh37 chr7: 147,044,513-147,044,572 CNTNAP2
    nsv6636153copy number variation1nstd102humanUncertain significance GRCh38 chrX: 29,803,177-29,803,323 , GRCh37 chrX: 29,821,294-29,821,440 IL1RAPL1
    nsv6636146copy number variation1nstd102humanUncertain significance GRCh37 chr17: 11,557,371-11,557,691 , GRCh38 chr17: 11,654,054-11,654,374 DNAH9
    nsv6636136copy number variation1nstd102humanUncertain significance GRCh37 chr18: 46,816,093-46,816,160 , GRCh38 chr18: 49,289,723-49,289,790 DYM
    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