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 101

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3880243copy number variation1nstd102humanLikely benign GRCh37 chr9: 17,295,644-17,364,986 , GRCh38 chr9: 17,295,646-17,364,988 CNTLN
    nsv4675666copy number variation1nstd102humanLikely benign GRCh37 chr9: 17,350,842-17,419,424 , GRCh38.p12 chr9: 17,350,844-17,419,426 CNTLN
    nsv3882123copy number variation1nstd102humanLikely benign GRCh37 chr9: 17,298,850-17,357,754 , GRCh38 chr9: 17,298,852-17,357,756 CNTLN
    nsv3895765copy number variation1nstd102humanBenign GRCh37 chr9: 17,260,525-17,296,630 , GRCh38.p12 chr9: 17,260,527-17,296,632 CNTLN
    nsv4729597copy number variation1nstd102humanLikely benign GRCh37 chr9: 17,053,143-17,185,702 , GRCh38.p12 chr9: 17,053,145-17,185,704 CNTLN, RPL31P42, 1 more genes
    nsv4728815copy number variation1nstd102humanLikely benign GRCh37 chr9: 17,165,697-17,708,155 , GRCh38.p12 chr9: 17,165,699-17,708,157 CNTLN, PABPC1P11, 3 more genes
    nsv3924091copy number variation1nstd102humanUncertain significance NCBI36 chr9: 16,907,756-17,157,391 , GRCh37.p13 chr9: 16,917,756-17,167,391 , GRCh38.p12 chr9: 16,917,758-17,167,393 CNTLN, RN7SL720P, 2 more genes
    nsv3894328copy number variation1nstd102humanUncertain significance GRCh37 chr9: 16,931,294-17,138,176 , GRCh38.p12 chr9: 16,931,296-17,138,178 CNTLN, LOC105375983, 2 more genes
    nsv3920950copy number variation1nstd102humanPathogenic NCBI36 chr9: 194,104-18,872,279 , GRCh37 chr9: 204,104-18,882,279 , GRCh38 chr9: 204,104-18,882,281 CNTLN, RPL4P5, 193 more genes
    nsv3910019copy number variation1nstd102humanPathogenic GRCh38 chr9: 220,253-18,708,805 , NCBI36 chr9: 210,253-18,698,803 , GRCh37 chr9: 220,253-18,708,803 CNTLN, LOC107987049, 191 more genes
    nsv5381767copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,654,812 , GRCh38.p12 chr9: 204,193-18,654,814 CNTLN, ACTG1P14, 191 more genes
    nsv4768366copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,073,357 , GRCh38.p12 chr9: 204,193-18,073,359 CNTLN, DOCK8-AS1, 186 more genes
    nsv3910119copy number variation1nstd102humanPathogenic NCBI36 chr9: 194,193-18,063,357 , GRCh38 chr9: 204,193-18,073,359 , GRCh37 chr9: 204,193-18,073,357 CNTLN, RNA5SP279, 186 more genes
    nsv3917303copy number variation1nstd102humanPathogenic GRCh38 chr9: 220,253-18,073,359 , GRCh37 chr9: 220,253-18,073,357 , NCBI36 chr9: 210,253-18,063,357 CNTLN, DMAC1, 185 more genes
    nsv4674929copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-17,789,410 , GRCh38.p12 chr9: 203,861-17,789,412 CNTLN, LINC02851, 184 more genes
    nsv3905168copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-17,655,298 , GRCh38.p12 chr9: 203,861-17,655,300 CNTLN, RANBP6, 184 more genes
    nsv3899178copy number variation1nstd102humanPathogenic GRCh37 chr9: 213,161-17,496,750 , GRCh38.p12 chr9: 213,161-17,496,752 CNTLN, GLIS3, 181 more genes
    nsv6315395copy number variation1nstd102humanPathogenic GRCh37 chr9: 4,992,582-19,322,101 , GRCh38.p12 chr9: 4,992,582-19,322,103 CNTLN, FREM1, 142 more genes
    nsv3921658copy number variation1nstd102humanPathogenic GRCh38 chr9: 9,661,633-18,034,356 , GRCh37 chr9: 9,661,633-18,034,354 , NCBI36 chr9: 9,651,633-18,024,354 CNTLN, LURAP1L, 67 more genes
    nsv3914995copy number variation1nstd102humanPathogenic GRCh37 chr9: 11,086,096-17,636,669 , NCBI36 chr9: 11,076,096-17,626,669 , GRCh38 chr9: 11,086,096-17,636,671 CNTLN, CLCN3P1, 60 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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