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 218

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv5969089insertion1nstd209human GRCh38 chr21: 30,614,184-30,614,184 , GRCh37.p13 chr21: 31,986,503-31,986,503 KRTAP6-1
    nsv5543843copy number variation1nstd206human GRCh38 chr21: 30,603,727-30,614,083 , GRCh37.p13 chr21: 31,976,046-31,986,402 KRTAP6-1
    nsv5539790insertion1nstd206human GRCh38 chr21: 5,227,438-39,583,816 , GRCh37.p13 chr21: 10,697,897-44,966,043 , LOC100419041, 557 more genes
    nsv5323906inversion1nstd204human GRCh37.p13 chr21: 30,417,326-35,280,637 , GRCh38.p13 chr21: 29,045,005-33,908,333 , ATP5PO, 129 more genes
    nsv5029336copy number variation1nstd200human GRCh38 chr21: 30,571,658-30,938,435 , GRCh37.p13 chr21: 31,943,977-32,310,754 KRTAP20-3, KRTAP8-1, 17 more genes
    nsv5023498copy number variation1nstd200human GRCh38 chr21: 30,513,966-30,688,897 , GRCh37.p13 chr21: 31,886,284-32,061,215 KRTAP20-1, KRTAP20-3, 11 more genes
    nsv5023174copy number variation1nstd200human GRCh38 chr21: 22,907,052-31,032,550 , GRCh37.p13 chr21: 24,279,373-32,404,869 , KRTAP13-1, 136 more genes
    nsv4863069copy number variation1nstd200human GRCh37 chr21: 31,886,284-32,061,215 , GRCh38.p12 chr21: 30,513,966-30,688,897 KRTAP6-3, KRTAP22-2, 11 more genes
    nsv4730021copy number variation1nstd102humanPathogenic GRCh37 chr21: 14,629,063-48,090,317 , GRCh38.p12 chr21: 13,256,742-46,670,405 SLX9, LOC105372750, 619 more genes
    nsv4729884copy number variation1nstd102humanUncertain significance GRCh37 chr21: 31,119,490-32,484,078 , GRCh38.p12 chr21: 29,747,171-31,111,760 KRTAP20-2, KRTAP6-3, 52 more genes
    nsv4684335copy number variation1nstd102humanUncertain significance GRCh37 chr21: 31,172,702-32,008,007 , GRCh38.p12 chr21: 29,800,385-30,635,688 KRTAP19-6, GRIK1, 35 more genes
    nsv4679058copy number variation1nstd189human GRCh37.p13 chr21: 14,468,835-48,129,895 , GRCh38.p12 chr21: 13,096,514-46,699,983 , ADARB1, 652 more genes
    nsv4676196copy number variation1nstd102humanPathogenic GRCh37 chr21: 31,711,916-34,632,473 , GRCh38.p12 chr21: 30,339,598-33,260,168 OLIG2, LOC105372787, 83 more genes
    nsv4676178copy number variation1nstd102humanPathogenic GRCh37 chr21: 27,826,100-32,468,109 , GRCh38.p12 chr21: 26,453,781-31,095,791 GRIK1-AS2, NCSTNP1, 94 more genes
    nsv4676117copy number variation1nstd102humanLikely benign GRCh37 chr21: 31,171,624-32,002,762 , GRCh38.p12 chr21: 29,799,307-30,630,443 KRTAP19-9P, KRTAP19-4, 34 more genes
    nsv4457773copy number variation2nstd102humanUncertain significance GRCh37 chr21: 31,171,623-32,010,342 , GRCh38.p12 chr21: 29,799,306-30,638,023 LOC105372772, MIR4327, 35 more genes
    nsv4385813copy number variation1nstd173human GRCh37 chr21: 15,006,458-48,097,384 , GRCh38.p12 chr21: 13,634,137-46,677,472 , GET1, 639 more genes
    nsv4382575copy number variation2nstd173human GRCh37 chr21: 15,006,458-48,097,372 , GRCh38.p12 chr21: 13,634,137-46,677,460 , CBR3-AS1, 639 more genes
    nsv4378831copy number variation1nstd173human GRCh37 chr21: 15,006,458-48,097,384 , GRCh38.p12 chr21: 13,634,137-46,677,472 , LOC105369299, 639 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