HGDP00650 AND nstd54 - dbVar - NCBI

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Items: 11

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Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv603870	copy number variation	45	nstd54	human		NCBI36 chr6: 79,029,920-79,098,352 , GRCh37.p13 chr6: 78,973,201-79,041,633 , GRCh38.p12 chr6: 78,263,484-78,331,916	LOC105377865
nsv589142	copy number variation	2	nstd54	human		NCBI36 chr22: 46,089,479-46,127,214 , GRCh37.p13 chr22: 47,710,815-47,748,550 , GRCh38.p12 chr22: 47,315,065-47,352,800	LOC339685
nsv610740	copy number variation	2	nstd54	human		NCBI36 chr8: 18,898,220-18,905,763 , GRCh37.p13 chr8: 18,853,940-18,861,483 , GRCh38.p12 chr8: 18,996,430-19,003,973	PSD3, LOC105379303
nsv609610	copy number variation	2	nstd54	human		NCBI36 chr8: 2,128,549-2,139,361 , GRCh37.p13 chr8\|NW_003571042.1: 175,753-186,565 , GRCh37.p13 chr8: 2,141,142-2,151,954 , GRCh38.p12 chr8\|NT_187576.1: 376,352-387,164 , GRCh38.p12 chr8: 2,193,611-2,204,315	LOC105377782, LOC105377781
nsv550755	copy number variation	158	nstd54	human		NCBI36 chr10: 47,013,328-47,173,619 , GRCh37.p13 chr10\|NW_003871068.1: 443,201-589,544 , GRCh37.p13 chr10: 47,543,322-47,689,665 , GRCh38.p12 chr10: 46,172,086-46,332,377	AHCYP1, LOC105378577, 2 more genes
nsv566984	copy number variation	3	nstd54	human		NCBI36 chr14: 105,997,070-106,111,905 , GRCh37.p13 chr14\|NW_004166863.1: 1,133,268-1,248,043 , GRCh37.p13 chr14: 106,926,025-107,040,860 , GRCh38.p12 chr14: 106,470,101-106,584,876	IGHV3-48, IGHVIII-47-1, 19 more genes
nsv588546	copy number variation	1	nstd54	human		NCBI36 chr22: 21,384,614-21,484,058 , GRCh37.p13 chr22: 23,054,614-23,154,058 , GRCh38.p12 chr22: 22,712,129-22,811,561	IGLV2-18, IGLV3-19, 14 more genes
nsv588584	copy number variation	4	nstd54	human		NCBI36 chr22: 21,502,190-21,570,027 , GRCh37.p13 chr22: 23,172,190-23,240,027 , GRCh38.p12 chr22: 22,830,010-22,897,847	IGLV2-5, IGLV3-4, 13 more genes
nsv584259	copy number variation	10	nstd54	human		NCBI36 chr2: 208,064,026-208,066,083 , GRCh37.p13 chr2: 208,355,781-208,357,838 , GRCh38.p12 chr2: 207,491,057-207,493,114	0
nsv611144	copy number variation	5	nstd54	human		NCBI36 chr8: 43,143,782-43,910,848 , GRCh37.p13 chr8: 43,024,625-43,791,691 , GRCh38.p12 chr8: 43,169,482-43,936,548	CYP4F44P, AFG3L2P1, 10 more genes
nsv564961	copy number variation	1	nstd54	human		NCBI36 chr14: 66,802,614-67,173,533 , GRCh37.p13 chr14: 67,732,861-68,103,780 , GRCh38.p12 chr14: 67,266,144-67,637,063	TMEM229B, , 11 more genes

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