NA18980 AND nstd4 - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv10097	copy number variation	11	nstd4	human	NCBI35 chr2: 97,279,637-97,339,539 , GRCh37.p13 chr2: 97,857,763-97,917,674 , GRCh38.p12 chr2: 97,192,026-97,251,937	ANKRD36
nsv10093	copy number variation	2	nstd4	human	NCBI35 chr2: 95,946,033-96,005,209 , GRCh37.p13 chr2: 96,524,159-96,583,335 , GRCh38.p12 chr2: 95,858,411-95,917,587	ANKRD36C
nsv9568	copy number variation	27	nstd4	human	NCBI35 chr17: 42,968,660-43,027,772 , GRCh37.p13 chr17: 45,613,661-45,672,773 , GRCh38.p12 chr17: 47,536,295-47,595,407	NPEPPS
nsv8649	copy number variation	26	nstd4	human	NCBI35 chr10: 51,064,677-51,177,185 , GRCh37.p13 chr10\|NW_003871068.1: 359,758-418,091 , GRCh37.p13 chr10: 51,394,671-51,507,179 , GRCh38.p12 chr10: 46,088,643-46,146,976	AGAP7P
nsv8616	copy number variation	23	nstd4	human	NCBI35 chr10: 37,482,743-37,530,033 , GRCh37.p13 chr10: 37,442,737-37,490,027 , GRCh38.p12 chr10: 37,153,809-37,201,099	ANKRD30A
nsv10534	copy number variation	5	nstd4	human	NCBI35 chr4: 92,323,778-92,366,360 , GRCh37.p13 chr4: 91,966,600-92,009,182 , GRCh38.p12 chr4: 91,045,449-91,088,031	CCSER1
nsv9477	copy number variation	13	nstd4	human	NCBI35 chr16: 88,163,792-88,202,556 , GRCh37.p13 chr16: 89,636,291-89,675,055 , GRCh38.p12 chr16: 89,569,883-89,608,647	CPNE7
nsv9445	copy number variation	28	nstd4	human	NCBI35 chr16: 54,351,821-54,381,093 , GRCh37.p13 chr16: 55,794,320-55,823,592 , GRCh38.p12 chr16: 55,760,408-55,789,680	CES1P1
nsv8265	copy number variation	26	nstd4	human	NCBI35 chr8: 2,232,990-2,257,526 , GRCh37.p13 chr8\|NW_003571042.1: 280,194-304,730 , GRCh37.p13 chr8: 2,245,583-2,270,119 , GRCh38.p12 chr8\|NT_187576.1: 480,793-505,329	LOC105377783
nsv10172	copy number variation	5	nstd4	human	NCBI35 chr2: 131,236,965-131,270,301 , GRCh37.p13 chr2: 132,008,464-132,032,624 , GRCh38.p12 chr2: 131,250,891-131,275,103	POTEE
nsv8668	copy number variation	29	nstd4	human	NCBI35 chr10: 56,115,764-56,139,619 , GRCh37.p13 chr10: 56,445,758-56,469,613 , GRCh38.p12 chr10: 54,685,998-54,709,853	PCDH15
nsv10759	copy number variation	18	nstd4	human	NCBI35 chr5: 150,181,427-150,204,688 , GRCh37.p13 chr5: 150,201,234-150,224,495 , GRCh38.p12 chr5: 150,821,672-150,844,933	IRGM
nsv8872	copy number variation	23	nstd4	human	NCBI35 chr11: 106,733,574-106,754,830 , GRCh37.p13 chr11: 107,228,364-107,249,620 , GRCh38.p12 chr11: 107,357,638-107,378,894	CWF19L2
nsv8121	copy number variation	24	nstd4	human	NCBI35 chr7: 64,026,367-64,046,571 , GRCh37.p13 chr7: 64,582,217-64,602,421 , GRCh38.p12 chr7: 65,121,839-65,142,043	INTS4P1
nsv8260	copy number variation	24	nstd4	human	NCBI35 chr8: 1,325,775-1,344,224 , GRCh37.p13 chr8: 1,338,368-1,356,817 , GRCh38.p12 chr8: 1,390,202-1,408,651 , GRCh38.p12 chr8\|NT_187654.1: 486-18,935	DLGAP2
nsv8444	copy number variation	5	nstd4	human	NCBI35 chr9: 33,782,372-33,797,431 , GRCh37.p13 chr9: 33,792,372-33,807,431 , GRCh38.p12 chr9: 33,792,374-33,807,433	PRSS3
nsv8891	copy number variation	7	nstd4	human	NCBI35 chr1: 226,114,786-226,129,759 , GRCh37.p13 chr1: 229,808,051-229,823,024 , GRCh38.p12 chr1: 229,672,304-229,687,277	KIAA1191P3
nsv10712	copy number variation	30	nstd4	human	NCBI35 chr5: 81,455,614-81,470,280 , GRCh37.p13 chr5: 81,419,858-81,434,524 , GRCh38.p12 chr5: 82,124,039-82,138,705	ATG10
nsv10163	copy number variation	5	nstd4	human	NCBI35 chr2: 130,549,037-130,563,114 , GRCh37.p13 chr2: 130,832,807-130,846,884 , GRCh38.p12 chr2: 130,075,234-130,089,311	POTEF
nsv10169	copy number variation	9	nstd4	human	NCBI35 chr2: 130,883,955-130,897,878 , GRCh37.p13 chr2: 131,167,725-131,181,648 , GRCh38.p12 chr2: 130,410,152-130,424,075	FAR2P2

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Study Type

Subject Phenotype Status

Additional filters

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Items: 1 to 20 of 441

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Number of Variants: 20

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