U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Nucleotide

Items: 6

    loading data ...

    Number of Variants: 6

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6625250copy number variation1nstd224human GRCh37 chr19: 54,962,374-55,451,378 , GRCh38.p12 chr19: 54,451,197-54,911,985 , GRCh38.p12 chr19|NT_187693.1: 433,488-894,467 , GRCh38.p12 chr19|NW_003571061.2: 363,080-652,171 , GRCh38.p12 chr19|NW_003571060.1: 355,882-844,362 , GRCh38.p12 chr19|NW_003571054.1: 357,709-843,408 , GRCh38.p12 chr19|NT_187636.1: 3-248,807 , GRCh38.p12 chr19|NT_187675.1: 4-282,224 , GRCh38.p12 chr19|NW_016107303.1: 1-293,522 KIR2DL4, KIR2DS3, 44 more genes
    nsv3894802copy number variation1nstd102humanBenign GRCh37 chr19: 55,343,039-55,606,944 , GRCh38.p12 chr19|NW_003571059.2: 763,398-1,002,683 , GRCh38.p12 chr19|NT_187636.1: 3-154,867 , GRCh38.p12 chr19|NT_187693.1: 894,468-1,066,800 , GRCh38.p12 chr19|NW_003571061.2: 609,417-796,479 , GRCh38.p12 chr19|NW_003571057.2: 904,779-1,091,841 , GRCh38.p12 chr19|NW_003571058.2: 819,634-1,066,390 , GRCh38.p12 chr19|NW_003571060.1: 735,953-987,100 , GRCh38.p12 chr19|NT_187675.1: 90,883-282,224 , GRCh38.p12 chr19: 54,911,986-55,095,576 , GRCh38.p12 chr19|NW_003571056.2: 811,616-1,064,304 , GRCh38.p12 chr19|NW_016107310.1: 79,866-223,118 , GRCh38.p12 chr19|NW_003571055.2: 481,924-729,520 , GRCh38.p12 chr19|NW_003571054.1: 800,654-987,716 PPP1R12C, RDH13, 21 more genes
    nsv2755100copy number variation1nstd130human NCBI36 chr19: 59,654,186-60,141,567 , GRCh37.p13 chr19|NW_004166865.1: 667,012-912,755 , GRCh38.p12 chr19: 54,451,197-54,911,985 , GRCh38.p12 chr19|NT_187693.1: 433,488-894,467 , GRCh38.p12 chr19|NW_003571061.2: 363,080-650,548 , GRCh38.p12 chr19|NW_003571060.1: 355,882-842,739 , GRCh38.p12 chr19|NW_003571054.1: 357,709-841,785 , GRCh38.p12 chr19|NT_187636.1: 3-248,807 , GRCh38.p12 chr19|NT_187675.1: 4-282,224 , GRCh38.p12 chr19|NW_016107303.1: 1-293,522 NLRP7, LAIR2, 44 more genes
    nsv2750201copy number variation2nstd130human NCBI36 chr19: 59,654,186-60,143,609 , GRCh37.p13 chr19|NW_004166865.1: 667,012-914,797 , GRCh38.p12 chr19: 54,451,197-54,911,985 , GRCh38.p12 chr19|NT_187693.1: 433,488-894,467 , GRCh38.p12 chr19|NW_003571061.2: 363,080-652,590 , GRCh38.p12 chr19|NW_003571060.1: 355,882-844,781 , GRCh38.p12 chr19|NW_003571054.1: 357,709-843,827 , GRCh38.p12 chr19|NT_187636.1: 3-248,807 , GRCh38.p12 chr19|NT_187675.1: 4-282,224 , GRCh38.p12 chr19|NW_016107303.1: 1-293,522 KIR2DP1, KIR2DL4, 44 more genes
    nsv1194440copy number variation2nstd113human NCBI36 chr19: 59,654,889-60,141,416 , GRCh37.p13 chr19|NW_004166865.1: 667,012-912,604 , GRCh38.p12 chr19: 54,451,900-54,911,985 , GRCh38.p12 chr19|NT_187693.1: 434,191-894,467 , GRCh38.p12 chr19|NW_003571061.2: 363,080-650,397 , GRCh38.p12 chr19|NW_003571060.1: 356,585-842,588 , GRCh38.p12 chr19|NW_003571054.1: 358,412-841,634 , GRCh38.p12 chr19|NT_187636.1: 3-248,807 , GRCh38.p12 chr19|NT_187675.1: 4-282,224 , GRCh38.p12 chr19|NW_016107303.1: 1-293,522 KIR2DL2, KIR2DS5, 44 more genes
    nsv137444copy number variation1nstd6human NCBI35 chr19: 59,917,958-59,917,958 , GRCh37.p13 chr19|NW_003571060.1: 619,034-619,034 , GRCh37.p13 chr19|NW_003571061.1: 440,705-440,705 , GRCh37.p13 chr19: 55,226,146-55,226,146 , GRCh37.p13 chr19|NW_003571054.1: 620,328-620,328 , GRCh38.p12 chr19|NT_187640.1: 187,972-187,972 , GRCh38.p12 chr19|NT_187670.1: 168,249-168,249 , GRCh38.p12 chr19|NT_187673.1: 154,434-154,434 , GRCh38.p12 chr19|NT_187674.1: 1,487-1,487 , GRCh38.p12 chr19|NT_187675.1: 13,203-13,203 , GRCh38.p12 chr19|NT_187686.1: 199,464-199,464 , GRCh38.p12 chr19|NW_003571054.1: 620,328-620,328 , GRCh38.p12 chr19|NT_187637.1: 154,132-154,132 , GRCh38.p12 chr19|NT_187638.1: 140,781-140,781 , GRCh38.p12 chr19|NT_187643.1: 154,431-154,431 , GRCh38.p12 chr19|NT_187644.1: 168,232-168,232 , GRCh38.p12 chr19|NT_187668.1: 188,927-188,927 , GRCh38.p12 chr19|NT_187687.1: 154,270-154,270 , GRCh38.p12 chr19|NT_187693.1: 697,260-697,260 , GRCh38.p12 chr19|NW_003571061.2: 440,706-440,706 , GRCh38.p12 chr19|NW_003571060.1: 619,034-619,034 , GRCh38.p12 chr19|NT_187639.1: 154,760-154,760 , GRCh38.p12 chr19|NT_187641.1: 193,761-193,761 , GRCh38.p12 chr19|NT_187645.1: 154,413-154,413 , GRCh38.p12 chr19|NT_187684.1: 184,506-184,506 , GRCh38.p12 chr19|NT_113949.2: 161,114-161,114 , GRCh38.p12 chr19|NT_187636.1: 232,540-232,540 , GRCh38.p12 chr19|NT_187642.1: 139,269-139,269 , GRCh38.p12 chr19|NT_187669.1: 154,397-154,397 , GRCh38.p12 chr19|NT_187677.1: 5,633-5,633 , GRCh38.p12 chr19|NT_187685.1: 153,881-153,881 LILRP2
    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