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 156

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099260copy number variation1nstd231human GRCh38.p12 chr1: 207,518,788-210,916,265 , GRCh37 chr1: 207,692,133-211,089,607 ADORA2BP1, ATP5MC2P1, 60 more genes
    nsv7095569copy number variation2nstd102humanUncertain significance GRCh37 chr1: 200,522,516-208,391,267 , GRCh38.p12 chr1: 200,553,388-208,217,922 TRK-TTT8-1, ADIPOR1, 228 more genes
    nsv7044092inversion1nstd229human GRCh38 chr1: 203,118,726-211,305,271 , GRCh37.p13 chr1: 203,087,854-211,478,613 LOC100420418, LINC00260, 201 more genes
    nsv6671668copy number variation1nstd229human GRCh38 chr1: 207,911,116-207,919,558 , GRCh37.p13 chr1: 208,084,461-208,092,903 LOC107985253, CD34
    nsv6669657copy number variation1nstd229human GRCh38 chr1: 207,877,982-207,886,105 , GRCh37.p13 chr1: 208,051,327-208,059,450 CD34
    nsv6669479copy number variation1nstd229human GRCh38 chr1: 207,905,701-207,907,500 , GRCh37.p13 chr1: 208,079,046-208,080,845 CD34
    nsv6660220copy number variation1nstd229human GRCh38 chr1: 207,738,001-208,652,200 , GRCh37.p13 chr1: 207,911,346-208,825,545 LOC105372887, LOC105372884, 14 more genes
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6554773inversion1nstd223human GRCh38 chr1: 204,500,842-208,290,127 , GRCh37.p13 chr1: 204,469,970-208,463,472 RNA5SP75, LOC105372869, 108 more genes
    nsv6310745copy number variation2nstd102humanUncertain significance GRCh37 chr1: 206,941,981-208,391,267 , GRCh38.p12 chr1: 206,768,636-208,217,922 PFKFB2, LOC105372878, 39 more genes
    nsv6133752copy number variation1nstd213human GRCh37 chr1: 207,160,000-210,270,001 , GRCh38.p12 chr1: 206,986,655-210,096,656 ADORA2BP1, C4BPA, 62 more genes
    nsv6133630copy number variation2nstd213human GRCh37 chr1: 206,490,000-223,720,001 , GRCh38.p12 chr1: 206,316,655-223,546,636 ATP5MC2P1, CENPF, 269 more genes
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5282634copy number variation1nstd204human GRCh38.p13 chr1: 207,890,898-207,891,025 , GRCh37.p13 chr1: 208,064,243-208,064,370 CD34
    nsv4898411copy number variation1nstd200human GRCh38 chr1: 207,895,002-207,895,111 , GRCh37.p13 chr1: 208,068,347-208,068,456 CD34
    nsv4898410copy number variation1nstd200human GRCh38 chr1: 207,890,908-207,891,016 , GRCh37.p13 chr1: 208,064,253-208,064,361 CD34
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4685577copy number variation1nstd102humannot provided GRCh37 chr1: 194,356,425-210,988,710 , GRCh38.p12 chr1: 194,387,295-210,815,368 SEPTIN14P12, LINC02602, 332 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